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rs6755560

From SNPedia

Orientationplus
Stabilizedplus
Make rs6755560(C;C)
Make rs6755560(C;T)
Make rs6755560(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position206853059
is asnp
is mentioned by
dbSNPrs6755560
ebirs6755560
HLIrs6755560
Exacrs6755560
Varsomers6755560
Maprs6755560
PheGenIrs6755560
hapmaprs6755560
1000 genomesrs6755560
hgdprs6755560
ensemblrs6755560
gopubmedrs6755560
geneviewrs6755560
scholarrs6755560
googlers6755560
pharmgkbrs6755560
gwascentralrs6755560
openSNPrs6755560
23andMers6755560
23andMe allrs6755560
SNP Nexus

SNPshotrs6755560
SNPdbers6755560
MSV3drs6755560
GWAS Ctlgrs6755560
GMAF0.2052
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