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Glutamate/all

From SNPedia

Transporters[edit]

excitatory amino acid transporters (EAATs)[edit]

  • SLC1A3/EAAT1 (glial, endothelial)
 On chromosomeChromosome positionIn geneSummary
rs137852620536,674,080SLC1A3
rs137852620(T;T)536,674,080SLC1A3common in clinvar
rs137852619(C;G)536,679,635SLC1A3Episodic ataxia, type 6
rs137852619(C;C)536,679,635SLC1A3common in clinvar
rs137852619536,679,635SLC1A3
rs138085358536,686,136SLC1A3
rs138085358(G;G)536,686,136SLC1A3common in clinvar
  • SLC1A2/EAAT2 (glial, endothelial)
 On chromosomeChromosome positionIn geneSummary
rs124190621135,228,123CD44
rs9273351135,228,971CD44
rs81931135,229,771CD44
rs118211021135,230,997CD44
rs11821102(G;G)1135,230,997CD44common in complete genomics
rs108363471135,231,586CD44
rs133471135,231,725CD44
rs13347(C;C)1135,231,725CD44common in complete genomics
rs47553921135,232,539CD44
rs107681221135,259,305SLC1A2
rs15702161135,260,787SLC1A2
rs38387961135,277,788SLC1A2
rs10421131135,286,822SLC1A2
rs7813792911135,292,512SLC1A2
rs7529491135,306,201SLC1A2
rs37940871135,308,068SLC1A2
rs8860379431135,315,079SLC1A2
rs886037943(T;T)1135,315,079SLC1A2common in clinvar
rs886037942(G;G)1135,315,089SLC1A2common in clinvar
rs8860379421135,315,089SLC1A2
rs40834821135,330,092SLC1A2
rs18853431135,355,043SLC1A2
rs19232981135,362,885SLC1A2
rs47562241135,369,861SLC1A2
rs45345571135,392,417SLC1A2
rs47554041135,404,103SLC1A2
rs43546681135,419,429SLC1A2
rs19232951135,421,061SLC1A2
  • SLC1A1/EAAT3 (glial, endothelial)
 On chromosomeChromosome positionIn geneSummary
rs10491734(A;A)94,482,7061.4x risk of early onset OCD
rs10491734(A;G)94,482,7061.4x risk of early onset OCD
rs1049173494,482,706
rs10491734(G;G)94,482,706normal
rs1692138594,507,513SLC1A1
rs702236994,527,752SLC1A1
rs785667594,555,305SLC1A1
SPATA6L
rs1097462094,557,296SLC1A1
SPATA6L
rs785881994,559,892SLC1A1
SPATA6L
rs222862294,564,432SLC1A1
SPATA6L
rs2228622(G;G)94,564,432SLC1A1
SPATA6L
common in clinvar
rs378041394,567,353SLC1A1
SPATA6L
rs378041294,572,480SLC1A1
SPATA6L
rs12682807(A;A)94,574,022SLC1A1
SPATA6L
common in clinvar
rs1268280794,574,022SLC1A1
SPATA6L
rs301430(T;T)94,576,680SLC1A1
SPATA6L
common in clinvar
rs30143094,576,680SLC1A1
SPATA6L
rs587777697(I;I)94,576,754SLC1A1
SPATA6L
common genotype
rs587777697(TCA;TCA)94,576,754SLC1A1
SPATA6L
common in clinvar
rs58777769794,576,754SLC1A1
SPATA6L
rs587777697(ATC;ATC)94,576,754SLC1A1
SPATA6L
common in clinvar
rs147178694,576,774SLC1A1
SPATA6L
rs75557938894,583,108SLC1A1
SPATA6L
rs755579388(G;G)94,583,108SLC1A1
SPATA6L
common in clinvar
rs58777769694,585,316SLC1A1
SPATA6L
rs587777696(C;C)94,585,316SLC1A1
SPATA6L
common in clinvar
rs308787994,586,808SLC1A1
SPATA6L
rs3087879(G;G)94,586,808SLC1A1
SPATA6L
common in clinvar
 On chromosomeChromosome positionIn geneSummary
rs3820201153,115,998SLC1A7
rs3820198153,326,979LRP8
LINC01771

vesicular glutamate transpoters (VGLUTs)[edit]

 On chromosomeChromosome positionIn geneSummary
rs10435581949,429,505SLC17A7
GFY
rs413087481954,636,725LILRB1
LOC107987461
rs10616841954,636,791LILRB1
LOC107987461
rs169854781954,636,798LILRB1
LOC107987461
rs415482131954,636,848LILRB1
LOC107987461
rs81012401954,636,880LILRB1
LOC107987461
 On chromosomeChromosome positionIn geneSummary
rs19005861122,365,894SLC17A6
 On chromosomeChromosome positionIn geneSummary
rs121918339(C;C)12100,396,373SLC17A8common in clinvar
rs12191833912100,396,373SLC17A8

Receptors[edit]

ionotropic[edit]

AMPA[edit]

 On chromosomeChromosome positionIn geneSummary
rs42621505152,908,893LINC01470
rs579176475153,124,378
rs14389495153,125,369
rs29100325153,160,794
rs5482945153,488,877GRIA1
rs21954505153,491,449GRIA1
rs100658135153,560,845GRIA1
rs126582025153,599,994GRIA1
rs19948625153,609,350GRIA1
rs121893625153,677,988GRIA1
rs68899095153,743,873GRIA1
rs68900575153,743,928GRIA1
rs49586765153,772,717GRIA1
rs49583515153,790,814GRIA1
rs100704475153,799,254GRIA1
 On chromosomeChromosome positionIn geneSummary
rs43025064157,317,678GRIA2
rs44030974157,364,445GRIA2
 On chromosomeChromosome positionIn geneSummary
rs989638X123,239,256GRIA3
rs144902457(T;T)X123,253,500GRIA3common in clinvar
rs144902457X123,253,500GRIA3
rs1034428(C;T)X123,303,197GRIA32.19x increased risk for schizophrenia in females
rs1034428(T;T)X123,303,197GRIA32.19x increased risk for schizophrenia in females
rs1034428X123,303,197GRIA3
rs1034428(C;C)X123,303,197GRIA3common/normal
rs4825476(A;A)X123,307,628GRIA3normal
rs4825476X123,307,628GRIA3
rs4825476(T;T)X123,307,628GRIA3
rs4825476(G;G)X123,307,628GRIA3
rs4825476(A;G)X123,307,628GRIA3normal
rs189437004X123,326,097GRIA3
rs139990565X123,326,163GRIA3
rs139990565(C;C)X123,326,163GRIA3common in clinvar
rs2227098X123,361,111GRIA3
rs587777361X123,427,951GRIA3
rs587777361(G;G)X123,427,951GRIA3common in clinvar
rs137852351X123,427,954GRIA3
rs137852351(C;C)X123,427,954GRIA3common in clinvar
rs1057521721X123,428,020GRIA3
rs1057521721(G;G)X123,428,020GRIA3common in clinvar
rs137852352X123,464,905GRIA3
rs137852352(T;T)X123,464,905GRIA3common in clinvar
rs1057521729X123,465,757GRIA3
rs1057521729(G;G)X123,465,757GRIA3common in clinvar
rs137852350(G;G)X123,482,856GRIA3common in clinvar
rs137852350X123,482,856GRIA3
 On chromosomeChromosome positionIn geneSummary
rs318133711104,994,711CASP5
rs965171311105,004,030CASP5
rs318117511105,004,534CASP5
rs318117111105,006,815CASP5
rs228265711105,007,076CASP5
rs50787911105,007,200CASP5Renal cancer risk
rs227641411105,008,835CASP5
rs55221711105,009,264CASP5
rs318131811105,009,313CASP5
rs55434411105,024,470CASP5
rs55620511105,027,281CASP1
rs556205(A;A)11105,027,281CASP1
rs53053711105,027,786CASP1
rs50119211105,029,658CASP1
rs58025311105,029,761CASP1
rs178588211105,052,348LOC107984381
rs1122661311105,101,791CARD17
rs317011105,642,334GRIA4
rs1160123911105,685,872GRIA4
rs76555621411105,933,765GRIA4

Kainate[edit]

 On chromosomeChromosome positionIn geneSummary
rs21863052129,543,953GRIK1
rs2832407(C;C)2129,595,188GRIK1
GRIK1-AS2
topiramate may work to reduce heavy drinking best for this genotype
rs28324072129,595,188GRIK1
GRIK1-AS2
rs3635982129,640,839GRIK1
rs3635122129,678,497GRIK1
rs726002(G;G)2129,678,973GRIK1
rs7260022129,678,973GRIK1
rs9331172129,728,478GRIK1
rs4558042129,773,850GRIK1
rs4586852129,805,194GRIK1
rs4573522129,872,161GRIK1
rs93054062130,013,925
rs9305406(A;A)2130,013,925common in complete genomics
rs28326162130,101,474
rs19439502130,107,534
 On chromosomeChromosome positionIn geneSummary
rs38102941947,228,572BBC3
MIR3191
rs3810294(C;C)1947,228,572BBC3
MIR3191
common in complete genomics
rs20328091947,232,959BBC3
rs2518224(A;A)6101,458,776GRIK2normal
rs2518224(A;C)6101,458,776GRIK2normal
rs2518224(C;C)6101,458,776GRIK2
rs25182246101,458,776GRIK2
rs65709896101,509,537GRIK2
rs93907546101,517,038GRIK2
rs4870836101,579,057GRIK2
rs749995448(C;C)6101,676,673GRIK2common in clinvar
rs7499954486101,676,673GRIK2
rs15569956101,869,470GRIK2
rs48402006101,879,428GRIK2
rs14171826101,885,466GRIK2
rs122076016101,907,992GRIK2
rs13350226102,018,522GRIK2
 On chromosomeChromosome positionIn geneSummary
rs514262136,820,874GRIK3
rs6691840136,859,876GRIK3
 On chromosomeChromosome positionIn geneSummary
rs208489811120,156,040
rs244424011120,169,734LOC107984399
rs424504011120,649,920GRIK4
rs1954787(C;C)11120,792,654GRIK4~10% more likely to respond to citalopram
rs195478711120,792,654GRIK4
rs1954787(C;T)11120,792,654GRIK4normal risk
rs1954787(T;T)11120,792,654GRIK4~10% less likely to respond to citalopram
rs1279775511120,938,751GRIK4
rs12797755(T;T)11120,938,751GRIK4common on affy axiom data
rs53451744711120,956,935GRIK4
LOC101929208
rs534517447(G;G)11120,956,935GRIK4
LOC101929208
common in clinvar
rs1280073411120,966,045GRIK4
rs86931269911120,986,102GRIK4
rs869312699(CTGGCGCAGGAGGCC;CTGGCGCAGGAGGCC)11120,986,102GRIK4common in clinvar
 On chromosomeChromosome positionIn geneSummary
rs80999391942,016,956GRIK5
rs3810294(C;C)1947,228,572BBC3
MIR3191
common in complete genomics
rs38102941947,228,572BBC3
MIR3191
rs20328091947,232,959BBC3

NMDA[edit]

 On chromosomeChromosome positionIn geneSummary
rs11146020(G;G)9137,138,632GRIN1
rs111460209137,138,632GRIN1
rs23013649137,140,083GRIN1
rs10647949879137,142,083GRIN1
rs1064794987(C;C)9137,142,083GRIN1common in clinvar
rs284899069137,143,947GRIN1
rs2007778509137,149,087GRIN1
rs8693128659137,156,676GRIN1
LOC105376328
rs869312865(G;G)9137,156,676GRIN1
LOC105376328
common in clinvar
rs1126442(G;G)9137,156,924GRIN1
LOC105376328
common in clinvar
rs11264429137,156,924GRIN1
LOC105376328
rs10647951589137,162,051GRIN1
rs1064795158(C;C)9137,162,051GRIN1common in clinvar
rs10647953379137,162,063GRIN1
rs1064795337(A;A)9137,162,063GRIN1common in clinvar
rs8788531439137,162,209GRIN1
rs878853143(C;C)9137,162,209GRIN1common in clinvar
rs7970450479137,162,510GRIN1
rs797045047(G;G)9137,162,510GRIN1common in clinvar
rs10605000469137,162,649GRIN1
rs1060500046(G;G)9137,162,649GRIN1common in clinvar
rs1064795455(A;A)9137,162,650GRIN1common in clinvar
rs10647954559137,162,650GRIN1
rs7716105689137,162,676GRIN1
rs10647970279137,162,681GRIN1
rs1064797027(C;C)9137,162,681GRIN1common in clinvar
rs3879066359137,162,710GRIN1
rs387906635(G;G)9137,162,710GRIN1common in clinvar
rs10575200559137,162,734GRIN1
rs1057520055(C;C)9137,162,734GRIN1common in clinvar
rs797044925(G;G)9137,163,668GRIN1common in clinvar
rs7970449259137,163,668GRIN1
 On chromosomeChromosome positionIn geneSummary
rs869312681(A;A)169,763,169GRIN2Acommon in clinvar
rs869312681169,763,169GRIN2A
rs886043129169,763,731GRIN2A
rs886043129(C;C)169,763,731GRIN2Acommon in clinvar
rs886041308169,763,843GRIN2A
rs886041308(T;T)169,763,843GRIN2Acommon in clinvar
rs796052556(G;G)169,764,203GRIN2Acommon in clinvar
rs796052556169,764,203GRIN2A
rs1064796658169,764,370GRIN2A
rs1064796658(C;C)169,764,370GRIN2Acommon in clinvar
rs886039239169,764,617GRIN2A
rs886039239(A;A)169,764,617GRIN2Acommon in clinvar
rs886042168(G;G)169,764,654GRIN2Acommon in clinvar
rs886042168169,764,654GRIN2A
rs796052552(C;C)169,764,696GRIN2Acommon in clinvar
rs796052552169,764,696GRIN2A
rs397518467(C;C)169,764,715GRIN2Acommon in clinvar
rs397518467169,764,715GRIN2A
rs11866328169,768,699GRIN2A
rs1064794679169,768,846GRIN2A
rs1064794679(G;G)169,768,846GRIN2Acommon in clinvar
rs1064796608169,768,996GRIN2A
rs1064796608(T;T)169,768,996GRIN2Acommon in clinvar
rs796052551169,768,997GRIN2A
rs796052551(A;A)169,768,997GRIN2Acommon in clinvar
rs1064795647169,769,019GRIN2A
rs1064795647(C;C)169,769,019GRIN2Acommon in clinvar
rs1064795143(TGTGGGTGATGGTAAGACC;TGTGGGTGATGGTAAGACC)169,798,269GRIN2A
LOC105371077
common in clinvar
rs1064795143169,798,269GRIN2A
LOC105371077
rs796052550169,798,436GRIN2A
LOC105371077
rs796052550(G;G)169,798,436GRIN2A
LOC105371077
common in clinvar
rs796052549(G;G)169,798,442GRIN2A
LOC105371077
common in clinvar
rs796052549169,798,442GRIN2A
LOC105371077
rs8058295169,817,529GRIN2A
rs762659685(C;C)169,822,286GRIN2Acommon in clinvar
rs762659685169,822,286GRIN2A
rs1057518070169,822,294GRIN2A
rs1057518070(T;T)169,822,294GRIN2Acommon in clinvar
rs796052563169,822,348GRIN2A
rs796052563(G;G)169,822,348GRIN2Acommon in clinvar
rs796052547(A;A)169,822,382GRIN2Acommon in clinvar
rs796052547169,822,382GRIN2A
rs397518472(C;C)169,822,391GRIN2Acommon in clinvar
rs397518472169,822,391GRIN2A
rs397518471169,829,476GRIN2A
rs397518471(T;T)169,829,476GRIN2Acommon in clinvar
rs397514557169,829,485GRIN2A
rs397514557(C;C)169,829,485GRIN2Acommon in clinvar
rs796052545169,829,487GRIN2A
rs796052545(A;A)169,829,487GRIN2Acommon in clinvar
... further results
 On chromosomeChromosome positionIn geneSummary
rs18055011213,561,125GRIN2B
rs1805501(A;A)1213,561,125GRIN2B
rs18055021213,561,247GRIN2B
rs18054761213,561,429GRIN2B
rs1805477(T;T)1213,561,795GRIN2Bcommon in clinvar
rs1805477(C;C)1213,561,795GRIN2Bcommon in complete genomics
rs18054771213,561,795GRIN2B
rs890(T;T)1213,562,374GRIN2Bcommon in clinvar
rs8901213,562,374GRIN2B
rs8766611671213,563,906GRIN2B
rs876661167(G;G)1213,563,906GRIN2Bcommon in clinvar
rs2014398801213,564,226GRIN2B
rs201439880(G;G)1213,564,226GRIN2Bcommon in clinvar
rs10575185201213,564,228GRIN2B
rs1057518520(-;-)1213,564,228GRIN2Bcommon in clinvar
rs876661102(AAG;AAG)1213,564,310GRIN2Bcommon in clinvar
rs8766611021213,564,310GRIN2B
rs1806201(G;G)1213,564,574GRIN2Bcommon in clinvar
rs18062011213,564,574GRIN2B
rs18062051213,566,469GRIN2B
rs7960525781213,567,034GRIN2B
rs796052578(C;C)1213,567,034GRIN2Bcommon in clinvar
rs8792539311213,567,084GRIN2B
rs879253931(C;C)1213,567,084GRIN2Bcommon in clinvar
rs1085307547(G;G)1213,567,108GRIN2Bcommon in clinvar
rs10853075471213,567,108GRIN2B
rs10647949791213,567,146GRIN2B
rs1064794979(G;G)1213,567,146GRIN2Bcommon in clinvar
rs7970448491213,567,164GRIN2B
rs797044849(G;G)1213,567,164GRIN2Bcommon in clinvar
rs8766610761213,567,171GRIN2B
rs876661076(A;A)1213,567,171GRIN2Bcommon in clinvar
rs8643095601213,567,193GRIN2B
rs864309560(C;C)1213,567,193GRIN2Bcommon in clinvar
rs1057518800(G;G)1213,567,228GRIN2Bcommon in clinvar
rs10575188001213,567,228GRIN2B
rs10575196121213,567,265GRIN2B
rs1057519612(A;A)1213,567,265GRIN2Bcommon in clinvar
rs10647967521213,569,848GRIN2B
rs1064796752(C;C)1213,569,848GRIN2Bcommon in clinvar
rs876661055(T;T)1213,569,937GRIN2Bcommon in clinvar
rs8766610551213,569,937GRIN2B
rs8766610641213,569,988GRIN2B
rs876661064(C;C)1213,569,988GRIN2Bcommon in clinvar
rs3981228241213,570,019GRIN2B
rs398122824(A;A)1213,570,019GRIN2Bcommon in clinvar
rs18061941213,570,193GRIN2B
rs10575189881213,571,859GRIN2B
rs1057518988(A;A)1213,571,859GRIN2Bcommon in clinvar
rs8766612191213,571,891GRIN2B
... further results
 On chromosomeChromosome positionIn geneSummary
rs886040861(G;G)1948,419,722GRIN2Dcommon in clinvar
rs8860408611948,419,722GRIN2D
 On chromosomeChromosome positionIn geneSummary
rs117884569101,585,868GRIN3A
rs14078779101,593,173GRIN3A
PPP3R2
LOC105376186
rs1407877(G;G)9101,593,173GRIN3A
PPP3R2
LOC105376186
common in complete genomics
rs171896329101,605,720GRIN3A
rs101216009101,615,721GRIN3A
rs10989591(C;C)9101,686,816GRIN3Acommon
rs109895919101,686,816GRIN3A
rs20506419101,727,085GRIN3A
 On chromosomeChromosome positionIn geneSummary
rs215912819950,380ARID3A
rs10666583191,004,897GRIN3B

delta[edit]

 On chromosomeChromosome positionIn geneSummary
rs70760961085,848,703GRID1
rs19705251085,875,167GRID1
rs767659681085,934,535GRID1
rs107884731085,980,996GRID1
rs79106201086,087,202GRID1
rs7910620(C;C)1086,087,202GRID1common in complete genomics
rs125736061086,122,545GRID1
rs112018871086,124,353GRID1
rs79156631086,154,279GRID1
rs79121611086,163,647GRID1
rs122575261086,169,086GRID1
rs122627541086,169,325GRID1
rs112019291086,184,814GRID1
rs26078391086,232,159GRID1
rs28143311086,233,584GRID1
rs112019851086,338,038GRID1
rs107495351086,344,769GRID1
rs79049851086,356,722GRID1
rs1194860961087,505,037MINPP1
rs119486096(C;C)1087,505,037MINPP1common in clinvar
rs1048941711087,508,507MINPP1
rs104894171(A;A)1087,508,507MINPP1common in clinvar
rs96642221087,578,876
rs9664222(C;C)1087,578,876common in complete genomics
rs108877411087,683,553PAPSS2
rs381140571087,687,132
rs1219089511087,709,311PAPSS2
rs121908951(C;C)1087,709,311PAPSS2common in clinvar
rs6062312411087,713,266PAPSS2
rs606231241(-;-)1087,713,266PAPSS2common in clinvar
rs6062312431087,714,142PAPSS2
rs606231243(-;-)1087,714,142PAPSS2common in clinvar
rs606231242(AGGTAGTGGAACTTCTGCA;AGGTAGTGGAACTTCTGCA)1087,714,840PAPSS2common in clinvar
rs6062312421087,714,840PAPSS2
rs7947277101087,714,864PAPSS2
rs794727710(G;G)1087,714,864PAPSS2common in clinvar
rs786200934(A;A)1087,715,006PAPSS2common in clinvar
rs7862009341087,715,006PAPSS2
rs1219089521087,727,403PAPSS2
rs121908952(C;C)1087,727,403PAPSS2common in clinvar
rs7862009331087,743,459PAPSS2
rs786200933(AG;AG)1087,743,459PAPSS2common in clinvar
rs121908950(C;C)1087,743,589PAPSS2common in clinvar
rs1219089501087,743,589PAPSS2
rs7970450991087,745,172PAPSS2
rs797045099(CATTC;CATTC)1087,745,172PAPSS2common in clinvar
rs112025861087,852,267
rs786204885(GCAAAAGCCGCA;GCAAAAGCCGCA)1087,863,274PTEN
KLLN
LOC101929706
common in clinvar
rs7862048851087,863,274PTEN
KLLN
LOC101929706
rs5877766751087,863,608PTEN
KLLN
LOC101929706
... further results
 On chromosomeChromosome positionIn geneSummary
rs7666831492,399,876GRID2
rs34144324492,590,245GRID2
rs1030757492,776,002GRID2
rs1905724493,461,245GRID2
rs750331613493,515,346GRID2
rs750331613(C;C)493,515,346GRID2common in clinvar
rs11097397493,947,701
rs13130787493,965,880
rs11097407494,224,984SMARCAD1
rs3106136494,232,198SMARCAD1
rs1057519613(G;G)494,253,672SMARCAD1common in clinvar
rs1057519613494,253,672SMARCAD1
rs1114167276494,253,673SMARCAD1
rs895436485(A;A)494,253,674SMARCAD1common in clinvar
rs895436485494,253,674SMARCAD1
rs1114167277494,253,676SMARCAD1
rs17021463494,303,661HPGDS
rs10008257494,435,177
rs2433320494,449,654
rs2433322494,458,590PDLIM5
rs2438146494,474,237PDLIM5
rs2452600494,575,731PDLIM5
rs4634230494,589,487PDLIM5
rs12500426494,593,458PDLIM5
rs966845(A;A)494,618,116PDLIM5common in complete genomics
rs966845494,618,116PDLIM5
rs7690296494,640,308PDLIM5
rs17021918494,641,726PDLIM5
rs951613494,651,548PDLIM5
rs13107595(A;A)494,657,437PDLIM5common in complete genomics
rs13107595494,657,437PDLIM5
rs11097432494,658,554PDLIM5
rs6532496494,659,253PDLIM5
rs1048627494,666,436PDLIM5
rs13133845494,673,465
rs17022027494,693,127
rs4699587(A;A)494,694,618
rs4699587494,694,618
rs10027628(T;T)494,722,806common genotype
rs10027628494,722,806
rs1859156494,912,883BMPR1B

metabotropic[edit]

group 1[edit]

 On chromosomeChromosome positionIn geneSummary
rs3629626146,312,682GRM1
rs69234926146,434,188GRM1
rs6923492(T;T)6146,434,188GRM1common in clinvar
rs132201416146,576,497
rs13220141(A;A)6146,576,497common genotype
rs22756066146,597,814ADGB
LOC101928661
 On chromosomeChromosome positionIn geneSummary
rs13863301188,086,259RAB38
rs1386330(T;T)1188,086,259RAB38common in complete genomics
rs3026681188,143,743RAB38
rs6824571188,216,364
rs104894215(G;G)1188,294,111CTSCcommon in clinvar
rs1048942151188,294,111CTSC
rs289375711188,294,163CTSC
rs28937571(T;T)1188,294,163CTSC
rs28937571(A;A)1188,294,163CTSCcommon in clinvar
rs587777532(T;T)1188,294,342CTSCcommon in clinvar
rs587777532(A;A)1188,294,342CTSCcommon in clinvar
rs587777532(I;I)1188,294,342CTSCcommon genotype
rs5877775321188,294,342CTSC
rs587777532(TG;TG)1188,294,342CTSCcommon in clinvar
rs5877766551188,294,351CTSC
rs587776655(T;T)1188,294,351CTSCcommon in clinvar
rs1048942111188,294,358CTSC
rs104894211(A;A)1188,294,358CTSCcommon in clinvar
rs1048942141188,294,497CTSC
rs104894214(G;G)1188,294,497CTSCcommon in clinvar
rs5877766541188,294,509CTSC
rs587776654(C;C)1188,294,509CTSCcommon in clinvar
rs587776654(G;G)1188,294,509CTSCcommon in clinvar
rs1048942081188,296,165CTSC
rs104894208(A;A)1188,296,165CTSCcommon in clinvar
rs1048942091188,296,166CTSC
rs104894209(C;C)1188,296,166CTSCcommon in clinvar
rs587777534(C;C)1188,296,207CTSCcommon in clinvar
rs5877775341188,296,207CTSC
rs2171151188,300,353CTSC
rs217116(A;A)1188,300,493CTSCcommon in clinvar
rs2171161188,300,493CTSC
rs104894207(A;A)1188,300,532CTSCcommon in clinvar
rs1048942071188,300,532CTSC
rs1048942061188,309,176CTSC
rs104894206(C;C)1188,309,176CTSCcommon in clinvar
rs2170861188,312,415CTSC
rs217086(A;A)1188,312,415CTSCcommon in clinvar
rs217086(G;G)1188,312,415CTSCcommon on affy axiom data
rs104894216(A;A)1188,312,493CTSCcommon in clinvar
rs1048942161188,312,493CTSC
rs1994748311188,335,052CTSC
rs199474831(T;T)1188,335,052CTSCcommon in clinvar
rs104894210(G;G)1188,337,557CTSC
LOC101929174
common in clinvar
rs1048942101188,337,557CTSC
LOC101929174
rs5877775331188,337,577CTSC
LOC101929174
rs587777533(A;A)1188,337,577CTSC
LOC101929174
common in clinvar
rs16914280(C;C)1188,588,556GRM5common in complete genomics
rs169142801188,588,556GRM5
rs71197491188,781,854GRM5
... further results

group 2[edit]

 On chromosomeChromosome positionIn geneSummary
rs41440786,145,233
rs2373124786,200,956
rs13222675786,282,105
rs2708553786,284,446
rs12673599786,334,718
rs274618786,642,700GRM3
rs274622786,643,624GRM3
rs148754219786,644,771GRM3
rs13242038786,685,104GRM3
rs724226786,696,058GRM3
rs2189814786,702,440GRM3
rs2189812786,719,683GRM3
rs917071786,724,465GRM3
rs6465084786,774,159GRM3
LOC105375382
rs2228595786,786,671GRM3
LOC107984122
rs2228595(C;C)786,786,671GRM3
LOC107984122
common in complete genomics
rs10234440786,791,061GRM3
LOC107984122
rs2237562786,792,916GRM3
LOC107984122
rs12704290786,798,310GRM3
rs1468412786,804,135GRM3
LOC107986814
rs17676277786,810,424GRM3
rs17161018786,815,615GRM3
rs2299225786,818,264GRM3
rs1989796786,844,997GRM3

group 3[edit]

 On chromosomeChromosome positionIn geneSummary
rs2229901634,022,670GRM4
rs1906953634,068,669GRM4
rs733457634,100,631GRM4
rs16894846634,101,146GRM4
rs7742369(A;A)634,197,944common in complete genomics
rs7742369634,197,944
 On chromosomeChromosome positionIn geneSummary
rs626386255178,983,005GRM6
rs62638625(G;G)5178,983,005GRM6common in clinvar
rs62638624(C;C)5178,986,132GRM6common in clinvar
rs626386245178,986,132GRM6
rs626382145178,986,393GRM6
rs62638214(C;C)5178,986,393GRM6common in clinvar
rs62638208(G;G)5178,986,689GRM6common in clinvar
rs626382085178,986,689GRM6
rs7489790615178,986,876GRM6
rs748979061(G;G)5178,986,876GRM6common in clinvar
rs1214343045178,989,075GRM6
rs121434304(T;T)5178,989,075GRM6common in clinvar
rs626382025178,994,497GRM6
rs62638202(G;G)5178,994,497GRM6common in clinvar
rs626381975178,994,808GRM6
rs62638197(C;C)5178,994,808GRM6common in clinvar
 On chromosomeChromosome positionIn geneSummary
rs374938036,861,610GRM7
rs3749380(G;G)36,861,610GRM7common/normal
rs48040936,968,394GRM7
rs1192886537,114,015GRM7
rs11928865(T;T)37,114,015GRM7common/normal
rs12491620(C;C)37,352,646GRM7common/normal
rs1249162037,352,646GRM7
rs1308059437,361,959GRM7
rs77986737,442,784GRM7
rs678201137,457,960GRM7
rs987068037,487,868GRM7
rs145010037,496,515GRM7
rs145009937,496,689GRM7
 On chromosomeChromosome positionIn geneSummary
rs5865867126,129,532
rs1179827307126,256,694
rs10345767126,423,377
rs7127237126,439,090GRM8
rs22994727126,580,415GRM8
rs176913947126,684,537GRM8
rs17691394(A;A)7126,684,537GRM8common in complete genomics
rs119711867126,797,843GRM8
rs121640897126,993,115GRM8
rs21881867126,997,797GRM8
rs178640927126,999,550GRM8
rs17864092(T;T)7126,999,550GRM8common in complete genomics
rs22377817127,034,996GRM8
rs1592377(A;A)7127,251,397GRM8
rs15923777127,251,397GRM8
rs1592377(A;C)7127,251,397GRM8