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rs2968864

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common on affy axiom data
Make rs2968864(A;G)
Make rs2968864(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position150925074
is asnp
is mentioned by
dbSNPrs2968864
ebirs2968864
HLIrs2968864
Exacrs2968864
Varsomers2968864
Maprs2968864
PheGenIrs2968864
hapmaprs2968864
1000 genomesrs2968864
hgdprs2968864
ensemblrs2968864
gopubmedrs2968864
geneviewrs2968864
scholarrs2968864
googlers2968864
pharmgkbrs2968864
gwascentralrs2968864
openSNPrs2968864
23andMers2968864
23andMe allrs2968864
SNP Nexus

SNPshotrs2968864
SNPdbers2968864
MSV3drs2968864
GWAS Ctlgrs2968864
GMAF0.1313
Max Magnitude0
? (A;A) (A;G) (G;G) 28

23andMe blog Influences QT interval

GWAS snp
PMID [PMID 19305408OA-icon.png]
Trait QT interval
Title Common variants at ten loci influence QT interval duation in the QTGEN Study
Risk Allele C
P-val 8E-16
Odds Ratio 1.40 [1.06-1.74] msec decrease



GET Evidence
rs2968864
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.132812
summary