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rs10919071

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common on affy axiom data
Make rs10919071(A;G)
Make rs10919071(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position169130245
GeneATP1B1
is asnp
is mentioned by
dbSNPrs10919071
ebirs10919071
HLIrs10919071
Exacrs10919071
Varsomers10919071
Maprs10919071
PheGenIrs10919071
hapmaprs10919071
1000 genomesrs10919071
hgdprs10919071
ensemblrs10919071
gopubmedrs10919071
geneviewrs10919071
scholarrs10919071
googlers10919071
pharmgkbrs10919071
gwascentralrs10919071
openSNPrs10919071
23andMers10919071
23andMe allrs10919071
SNP Nexus

SNPshotrs10919071
SNPdbers10919071
MSV3drs10919071
GWAS Ctlgrs10919071
GMAF0.0877
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19305409OA-icon.png]
Trait QT interval
Title Common variants at ten loci modulate the QT interval duration in the QTSCD Study
Risk Allele A
P-val 1E-15
Odds Ratio 2.05 [1.48-2.62] ms increase



[PMID 19305408OA-icon.png] Common variants at ten loci influence QT interval duration in the QTGEN Study.


GET Evidence
rs10919071
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.109375
summary