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rs1263173

From SNPedia

Orientationplus
Stabilizedplus
Make rs1263173(A;A)
Make rs1263173(A;G)
Make rs1263173(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position116810292
is asnp
is mentioned by
dbSNPrs1263173
dbSNP (classic)rs1263173
ClinGenrs1263173
ebirs1263173
HLIrs1263173
Exacrs1263173
Gnomadrs1263173
Varsomers1263173
LitVarrs1263173
Maprs1263173
PheGenIrs1263173
Biobankrs1263173
1000 genomesrs1263173
hgdprs1263173
ensemblrs1263173
geneviewrs1263173
scholarrs1263173
googlers1263173
pharmgkbrs1263173
gwascentralrs1263173
openSNPrs1263173
23andMers1263173
SNPshotrs1263173
SNPdbers1263173
MSV3drs1263173
GWAS Ctlgrs1263173
GMAF0.4394
Max Magnitude0
? (A;A) (A;G) (G;G) 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 A
P-val 2E-7
Odds Ratio 0.0873 [0.06-0.12] SD decrease