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rs1190739

From SNPedia

Orientationplus
Stabilizedplus
Make rs1190739(C;C)
Make rs1190739(C;T)
Make rs1190739(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position136973136
GeneLOC100132625
is asnp
is mentioned by
dbSNPrs1190739
ebirs1190739
HLIrs1190739
Exacrs1190739
Varsomers1190739
Maprs1190739
PheGenIrs1190739
hapmaprs1190739
1000 genomesrs1190739
hgdprs1190739
ensemblrs1190739
gopubmedrs1190739
geneviewrs1190739
scholarrs1190739
googlers1190739
pharmgkbrs1190739
gwascentralrs1190739
openSNPrs1190739
23andMers1190739
23andMe allrs1190739
SNP Nexus

SNPshotrs1190739
SNPdbers1190739
MSV3drs1190739
GWAS Ctlgrs1190739
GMAF0.1167
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21347282OA-icon.png]
Trait
Title Genome-Wide Association Study of Coronary Heart Disease and Its Risk Factors in 8,090 African Americans: The NHLBI CARe Project
Risk Allele T
P-val 0.000005
Odds Ratio 0.0731 [0.04-0.10] SD decrease