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rs13232179

From SNPedia

Orientationplus
Stabilizedplus
Make rs13232179(A;A)
Make rs13232179(A;T)
Make rs13232179(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position151423862
is asnp
is mentioned by
dbSNPrs13232179
ebirs13232179
HLIrs13232179
Exacrs13232179
Varsomers13232179
Maprs13232179
PheGenIrs13232179
hapmaprs13232179
1000 genomesrs13232179
hgdprs13232179
ensemblrs13232179
gopubmedrs13232179
geneviewrs13232179
scholarrs13232179
googlers13232179
pharmgkbrs13232179
gwascentralrs13232179
openSNPrs13232179
23andMers13232179
23andMe allrs13232179
SNP Nexus

SNPshotrs13232179
SNPdbers13232179
MSV3drs13232179
GWAS Ctlgrs13232179
GMAF0.2048
Max Magnitude
? (A;A) (A;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 A
P-val 0.000001
Odds Ratio 1.6700 [1.36-2.06]