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rs7173743

From SNPedia

Orientationplus
Stabilizedplus
Make rs7173743(C;C)
Make rs7173743(C;T)
Make rs7173743(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position78849442
is asnp
is mentioned by
dbSNPrs7173743
dbSNP (classic)rs7173743
ClinGenrs7173743
ebirs7173743
HLIrs7173743
Exacrs7173743
Gnomadrs7173743
Varsomers7173743
LitVarrs7173743
Maprs7173743
PheGenIrs7173743
Biobankrs7173743
1000 genomesrs7173743
hgdprs7173743
ensemblrs7173743
geneviewrs7173743
scholarrs7173743
googlers7173743
pharmgkbrs7173743
gwascentralrs7173743
openSNPrs7173743
23andMers7173743
SNPshotrs7173743
SNPdbers7173743
MSV3drs7173743
GWAS Ctlgrs7173743
Max Magnitude0
? (C;C) (C;T) (T;T) 28



[PMID 3679547OA-icon.png] Large-scale association analysis identifies new risk loci for coronary artery disease.

GWAS snp
PMID [PMID 24262325OA-icon.png]
Trait Coronary artery disease
Title Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.
Risk Allele C
P-val 7E-8
Odds Ratio 1.08 [1.05-1.11]