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rs7006687

From SNPedia

Orientationplus
Stabilizedplus
Make rs7006687(C;C)
Make rs7006687(C;T)
Make rs7006687(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position18376073
is asnp
is mentioned by
dbSNPrs7006687
ebirs7006687
HLIrs7006687
Exacrs7006687
Varsomers7006687
Maprs7006687
PheGenIrs7006687
hapmaprs7006687
1000 genomesrs7006687
hgdprs7006687
ensemblrs7006687
gopubmedrs7006687
geneviewrs7006687
scholarrs7006687
googlers7006687
pharmgkbrs7006687
gwascentralrs7006687
openSNPrs7006687
23andMers7006687
23andMe allrs7006687
SNP Nexus

SNPshotrs7006687
SNPdbers7006687
MSV3drs7006687
GWAS Ctlgrs7006687
GMAF0.4256
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 T
P-val 2E-6
Odds Ratio NR NR