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rs16856785

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs16856785(C;C)
Make rs16856785(C;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position162130497
GeneNOS1AP
is asnp
is mentioned by
dbSNPrs16856785
ebirs16856785
HLIrs16856785
Exacrs16856785
Varsomers16856785
Maprs16856785
PheGenIrs16856785
hapmaprs16856785
1000 genomesrs16856785
hgdprs16856785
ensemblrs16856785
gopubmedrs16856785
geneviewrs16856785
scholarrs16856785
googlers16856785
pharmgkbrs16856785
gwascentralrs16856785
openSNPrs16856785
23andMers16856785
23andMe allrs16856785
SNP Nexus

SNPshotrs16856785
SNPdbers16856785
MSV3drs16856785
GWAS Ctlgrs16856785
GMAF0.2603
Max Magnitude0
? (C;C) (C;G) (G;G) 28
[PMID 19180230OA-icon.png] rs16847548 and rs16856785 strongly associated with QT interval


[PMID 19204306OA-icon.png] Genetic variations in nitric oxide synthase 1 adaptor protein are associated with sudden cardiac death in US white community-based populations.