Disease: Long QT Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10800397
rs10800397
Entrez Id: 9722
Gene Symbol: NOS1AP
NOS1AP
CUI: C0023976
Disease:
Long QT Syndrome 		0.010 GeneticVariation BEFREE The rs10800397 SNP was significantly associated with dLQTS (odds ratio [OR]: 3.3, 99.95% confidence interval [CI]: 1.0 to 10.8, p = 3.7 × 10(-4)). 22682551 2012