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MYH9

From SNPedia

is agene
is mentioned by
Full namemyosin, heavy chain 9, non-muscle
EntrezGene4627
PheGenI4627
VariationViewer4627
ClinVarMYH9
GeneCardsMYH9
dbSNP4627
SADR4627
HugeNav4627
wikipediaMYH9
googleMYH9
gopubmedMYH9
EVSMYH9
HEFalMpMYH9
MyGene2MYH9
23andMeMYH9
UniProtP35579
EnsemblENSG00000100345
OMIM160775
# SNPs32
 Max MagnitudeChromosome positionSummary
rs1108978836,355,056
rs11912763036,288,676
rs121913655036,348,958
rs121913656036,295,526
rs121913657036,348,950
rs16996652036,300,203
rs2032487036,299,382
rs207173136,322,813
rs2269529036,288,308
rs2413396036,312,039
rs3752462036,314,138
rs4821480036,299,201
rs4821481036,299,896
rs5750248036,306,846
rs5750250036,312,438
rs587776808036,282,730
rs599528836,366,589
rs707836,281,868
rs727503284036,289,096
rs73585436,283,012
rs73909736,350,034
rs797044804036,291,990
rs80338826036,305,985
rs80338827036,305,984
rs80338828036,305,975
rs80338829036,295,069
rs80338830036,295,068
rs80338831036,292,060
rs80338834036,284,474
rs80338835036,282,754
rs876661302036,296,900
rs876661303036,296,899


Associated with deafness; DFNA17

[PMID 19177153] Polymorphisms in MYH9 are strongly associated with end-stage renal disease historically attributed to hypertension in African Americans