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rs10890920

From SNPedia

Orientationplus
Stabilizedplus
Make rs10890920(A;A)
Make rs10890920(A;G)
Make rs10890920(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position109002392
is asnp
is mentioned by
dbSNPrs10890920
dbSNP (classic)rs10890920
ClinGenrs10890920
ebirs10890920
HLIrs10890920
Exacrs10890920
Gnomadrs10890920
Varsomers10890920
LitVarrs10890920
Maprs10890920
PheGenIrs10890920
Biobankrs10890920
1000 genomesrs10890920
hgdprs10890920
ensemblrs10890920
geneviewrs10890920
scholarrs10890920
googlers10890920
pharmgkbrs10890920
gwascentralrs10890920
openSNPrs10890920
23andMers10890920
SNPshotrs10890920
SNPdbers10890920
MSV3drs10890920
GWAS Ctlgrs10890920
GMAF0.4972
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 23459443OA-icon.png]
Trait QT interval (interaction)
Title Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval.
Risk Allele A
P-val 3E-6
Odds Ratio NR NR