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rs6873793

From SNPedia

Orientationplus
Stabilizedplus
Make rs6873793(C;C)
Make rs6873793(C;T)
Make rs6873793(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position3092078
is asnp
is mentioned by
dbSNPrs6873793
ebirs6873793
HLIrs6873793
Exacrs6873793
Varsomers6873793
Maprs6873793
PheGenIrs6873793
hapmaprs6873793
1000 genomesrs6873793
hgdprs6873793
ensemblrs6873793
gopubmedrs6873793
geneviewrs6873793
scholarrs6873793
googlers6873793
pharmgkbrs6873793
gwascentralrs6873793
openSNPrs6873793
23andMers6873793
23andMe allrs6873793
SNP Nexus

SNPshotrs6873793
SNPdbers6873793
MSV3drs6873793
GWAS Ctlgrs6873793
GMAF0.494
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23166209OA-icon.png]
Trait QT interval
Title Impact of Ancestry and Common Genetic Variants on QT Interval in African Americans.
Risk Allele C
P-val 1E-6
Odds Ratio 1.47 [0.88-2.06] unit increase