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rs16857031

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs16857031(C;G)
Make rs16857031(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position162143120
GeneNOS1AP
is asnp
is mentioned by
dbSNPrs16857031
ebirs16857031
HLIrs16857031
Exacrs16857031
Varsomers16857031
Maprs16857031
PheGenIrs16857031
hapmaprs16857031
1000 genomesrs16857031
hgdprs16857031
ensemblrs16857031
gopubmedrs16857031
geneviewrs16857031
scholarrs16857031
googlers16857031
pharmgkbrs16857031
gwascentralrs16857031
openSNPrs16857031
23andMers16857031
23andMe allrs16857031
SNP Nexus

SNPshotrs16857031
SNPdbers16857031
MSV3drs16857031
GWAS Ctlgrs16857031
GMAF0.1997
Max Magnitude0
? (C;C) (C;G) (G;G) 28
23andMe blog Influences QT interval
GWAS snp
PMID [PMID 19305408OA-icon.png]
Trait QT interval
Title Common variants at ten loci influence QT interval duation in the QTGEN Study
Risk Allele G
P-val 1E-34
Odds Ratio


GET Evidence
rs16857031
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.210938
summary



[PMID 26600494] Analysis of SNP (single nucleotide polymorphism) multiplex markers related to sudden cardiac death in Brazilian families