Have questions? Visit https://www.reddit.com/r/SNPedia

rs3778872

From SNPedia

Orientationminus
Stabilizedminus
Make rs3778872(C;C)
Make rs3778872(C;G)
Make rs3778872(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position150972888
GeneKCNH2
is asnp
is mentioned by
dbSNPrs3778872
ebirs3778872
HLIrs3778872
Exacrs3778872
Varsomers3778872
Maprs3778872
PheGenIrs3778872
hapmaprs3778872
1000 genomesrs3778872
hgdprs3778872
ensemblrs3778872
gopubmedrs3778872
geneviewrs3778872
scholarrs3778872
googlers3778872
pharmgkbrs3778872
gwascentralrs3778872
openSNPrs3778872
23andMers3778872
23andMe allrs3778872
SNP Nexus

SNPshotrs3778872
SNPdbers3778872
MSV3drs3778872
GWAS Ctlgrs3778872
GMAF0.236
Max Magnitude
? (C;C) (C;G) (G;G) 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 3E-6
Odds Ratio 1.77 [1.04-2.50] unit decrease