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rs10027628

From SNPedia

Orientationplus
Stabilizedplus
Make rs10027628(C;C)
Make rs10027628(C;T)
Make rs10027628(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position94722806
is asnp
is mentioned by
dbSNPrs10027628
ebirs10027628
HLIrs10027628
Exacrs10027628
Varsomers10027628
Maprs10027628
PheGenIrs10027628
hapmaprs10027628
1000 genomesrs10027628
hgdprs10027628
ensemblrs10027628
gopubmedrs10027628
geneviewrs10027628
scholarrs10027628
googlers10027628
pharmgkbrs10027628
gwascentralrs10027628
openSNPrs10027628
23andMers10027628
23andMe allrs10027628
SNP Nexus

SNPshotrs10027628
SNPdbers10027628
MSV3drs10027628
GWAS Ctlgrs10027628
GMAF0.06887
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 6E-6
Odds Ratio 1.81 [1.05-2.57] unit decrease