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rs10919035

From SNPedia

Orientationplus
Stabilizedplus
Make rs10919035(C;C)
Make rs10919035(C;T)
Make rs10919035(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position162274222
GeneNOS1AP
is asnp
is mentioned by
dbSNPrs10919035
ebirs10919035
HLIrs10919035
Exacrs10919035
Varsomers10919035
Maprs10919035
PheGenIrs10919035
hapmaprs10919035
1000 genomesrs10919035
hgdprs10919035
ensemblrs10919035
gopubmedrs10919035
geneviewrs10919035
scholarrs10919035
googlers10919035
pharmgkbrs10919035
gwascentralrs10919035
openSNPrs10919035
23andMers10919035
23andMe allrs10919035
SNP Nexus

SNPshotrs10919035
SNPdbers10919035
MSV3drs10919035
GWAS Ctlgrs10919035
GMAF0.2603
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

[PMID 24922963] 163 Genetic Modifiers in Carriers of the SCN5A E1784K Mutation with Variable Phenotypic Expression - Long QT3 / Brugada Syndrome Overlap Disease