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rs7729539

From SNPedia

Orientationplus
Stabilizedplus
Make rs7729539(C;C)
Make rs7729539(C;T)
Make rs7729539(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position65121851
is asnp
is mentioned by
dbSNPrs7729539
ebirs7729539
HLIrs7729539
Exacrs7729539
Varsomers7729539
Maprs7729539
PheGenIrs7729539
hapmaprs7729539
1000 genomesrs7729539
hgdprs7729539
ensemblrs7729539
gopubmedrs7729539
geneviewrs7729539
scholarrs7729539
googlers7729539
pharmgkbrs7729539
gwascentralrs7729539
openSNPrs7729539
23andMers7729539
23andMe allrs7729539
SNP Nexus

SNPshotrs7729539
SNPdbers7729539
MSV3drs7729539
GWAS Ctlgrs7729539
GMAF0.01791
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 2.59 [1.55-3.63] unit decrease