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rs10800397

From SNPedia

Orientationplus
Stabilizedplus
Make rs10800397(C;C)
Make rs10800397(C;T)
Make rs10800397(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position162267300
GeneNOS1AP
is asnp
is mentioned by
dbSNPrs10800397
ebirs10800397
HLIrs10800397
Exacrs10800397
Varsomers10800397
Maprs10800397
PheGenIrs10800397
hapmaprs10800397
1000 genomesrs10800397
hgdprs10800397
ensemblrs10800397
gopubmedrs10800397
geneviewrs10800397
scholarrs10800397
googlers10800397
pharmgkbrs10800397
gwascentralrs10800397
openSNPrs10800397
23andMers10800397
23andMe allrs10800397
SNP Nexus

SNPshotrs10800397
SNPdbers10800397
MSV3drs10800397
GWAS Ctlgrs10800397
GMAF0.3104
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 22682551OA-icon.png] Common Variation in the NOS1AP Gene Is Associated With Drug-Induced QT Prolongation and Ventricular Arrhythmia