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rs2968863

From SNPedia

Orientationminus
Stabilizedplus
Make rs2968863(A;A)
Make rs2968863(A;G)
Make rs2968863(G;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150926049
is asnp
is mentioned by
dbSNPrs2968863
ebirs2968863
HLIrs2968863
Exacrs2968863
Varsomers2968863
Maprs2968863
PheGenIrs2968863
hapmaprs2968863
1000 genomesrs2968863
hgdprs2968863
ensemblrs2968863
gopubmedrs2968863
geneviewrs2968863
scholarrs2968863
googlers2968863
pharmgkbrs2968863
gwascentralrs2968863
openSNPrs2968863
23andMers2968863
23andMe allrs2968863
SNP Nexus

SNPshotrs2968863
SNPdbers2968863
MSV3drs2968863
GWAS Ctlgrs2968863
GMAF0.1345
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19305409OA-icon.png]
Trait QT interval
Title Common variants at ten loci modulate the QT interval duration in the QTSCD Study
Risk Allele T
P-val 2E-15
Odds Ratio 1.35 [0.90-1.80] ms decrease



GET Evidence
rs2968863
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.148438
summary