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NRXN1

From SNPedia
is agene
is mentioned by
Full nameneurexin 1
EntrezGene9378
PheGenI9378
VariationViewer9378
ClinVarNRXN1
GeneCardsNRXN1
dbSNP9378
DiseasesNRXN1
SADR9378
HugeNav9378
wikipediaNRXN1
googleNRXN1
gopubmedNRXN1
EVSNRXN1
HEFalMpNRXN1
MyGene2NRXN1
23andMeNRXN1
UniProtP58400
EnsemblENSG00000179915
OMIM600565
# SNPs22
 Max MagnitudeChromosome positionSummary
rs1002820022050,054,994
rs10176705050,517,636
rs1045881049,921,834
rs10490162051,020,519
rs1057520406050,091,496
rs1057521798050,497,380
rs1064795493051,028,155
rs11681792049,957,256
rs12467557051,015,132
rs12623467050,997,951
rs1356888050,288,880
rs17041183051,002,517
rs20245131.750,924,881
rs2193225050,852,344
rs2303298050,623,548
rs267606922050,496,039
rs3850333050,775,791
rs6721498050,485,874
rs675063450,533,365
rs6754640050,504,180
rs796052787050,496,087
rs886042846050,465,563

[PMID 18945720] among 2,977 schizophrenia patients and 33,746 controls, NRXN1 CNVs disrupting exons were significantly associated with a high odds ratio (OR 8.97, 95% CI 1.8-51.9, p = 0.0027) for schizophrenia