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rs1426063

From SNPedia

Orientationminus
Stabilizedplus
Make rs1426063(C;C)
Make rs1426063(C;T)
Make rs1426063(T;T)
ReferenceGRCh38 38.1/142
Chromosome4
Position75105711
is asnp
is mentioned by
dbSNPrs1426063
ebirs1426063
HLIrs1426063
Exacrs1426063
Varsomers1426063
Maprs1426063
PheGenIrs1426063
hapmaprs1426063
1000 genomesrs1426063
hgdprs1426063
ensemblrs1426063
gopubmedrs1426063
geneviewrs1426063
scholarrs1426063
googlers1426063
pharmgkbrs1426063
gwascentralrs1426063
openSNPrs1426063
23andMers1426063
23andMe allrs1426063
SNP Nexus

SNPshotrs1426063
SNPdbers1426063
MSV3drs1426063
GWAS Ctlgrs1426063
GMAF0.1786
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 A
P-val 8E-6
Odds Ratio 1.18 [0.67-1.69] unit decrease