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NRXN1

From SNPedia

is agene
is mentioned by
Full nameneurexin 1
EntrezGene9378
PheGenI9378
VariationViewer9378
ClinVarNRXN1
GeneCardsNRXN1
dbSNP9378
SADR9378
HugeNav9378
wikipediaNRXN1
googleNRXN1
gopubmedNRXN1
EVSNRXN1
HEFalMpNRXN1
MyGene2NRXN1
23andMeNRXN1
UniProtP58400
EnsemblENSG00000179915
OMIM600565
# SNPs17
 Max MagnitudeChromosome positionSummary
rs1017670550,517,636
rs104588149,921,834
rs1049016251,020,519
rs1168179249,957,256
rs12467557051,015,132
rs12623467050,997,951
rs135688850,288,880
rs17041183051,002,517
rs20245131.750,924,881
rs219322550,852,344
rs2303298050,623,548
rs267606922050,496,039
rs385033350,775,791
rs672149850,485,874
rs675063450,533,365
rs675464050,504,180
rs796052787050,496,087

[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