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rs1612141

From SNPedia

Orientationminus
Stabilizedminus
Make rs1612141(C;C)
Make rs1612141(C;T)
Make rs1612141(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position41233395
is asnp
is mentioned by
dbSNPrs1612141
ebirs1612141
HLIrs1612141
Exacrs1612141
Varsomers1612141
Maprs1612141
PheGenIrs1612141
hapmaprs1612141
1000 genomesrs1612141
hgdprs1612141
ensemblrs1612141
gopubmedrs1612141
geneviewrs1612141
scholarrs1612141
googlers1612141
pharmgkbrs1612141
gwascentralrs1612141
openSNPrs1612141
23andMers1612141
23andMe allrs1612141
SNP Nexus

SNPshotrs1612141
SNPdbers1612141
MSV3drs1612141
GWAS Ctlgrs1612141
GMAF0.2259
Max Magnitude
? (C;C) (C;T) (T;T) 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 5E-6
Odds Ratio NR NR