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rs7613868

From SNPedia

Orientationplus
Stabilizedplus
Make rs7613868(C;C)
Make rs7613868(C;T)
Make rs7613868(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position124023182
is asnp
is mentioned by
dbSNPrs7613868
ebirs7613868
HLIrs7613868
Exacrs7613868
Varsomers7613868
Maprs7613868
PheGenIrs7613868
hapmaprs7613868
1000 genomesrs7613868
hgdprs7613868
ensemblrs7613868
gopubmedrs7613868
geneviewrs7613868
scholarrs7613868
googlers7613868
pharmgkbrs7613868
gwascentralrs7613868
openSNPrs7613868
23andMers7613868
23andMe allrs7613868
SNP Nexus

SNPshotrs7613868
SNPdbers7613868
MSV3drs7613868
GWAS Ctlgrs7613868
GMAF0.4949
Max Magnitude
? (C;C) (C;T) (T;T) 28
Rs7613868
PubMed [PMID 17357071OA-icon.png]
Affy Probeset SNP_A-8580439
Affy Orientation same
On GW 5.0 0
Alleles A/B C/T
Ancestral T
Population Caucasian
Allele T
Case Freq. 0.37
Control Freq. 0.26
Odds Ratio Het
Odds Ratio Hom
Odds Ratio All 1.80
Disease Coronary artery disease (CAD)


rs7613868 increases susceptibility to Atherosclerosis 2.60 times for carriers of the T allele [PMID 17357071OA-icon.png]

rs7613868 increases susceptibility to Coronary artery disease 1.80 times for carriers of the T allele [PMID 17357071OA-icon.png]