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rs13015955

From SNPedia

Orientationplus
Stabilizedplus
Make rs13015955(A;A)
Make rs13015955(A;G)
Make rs13015955(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position22599287
is asnp
is mentioned by
dbSNPrs13015955
ebirs13015955
HLIrs13015955
Exacrs13015955
Varsomers13015955
Maprs13015955
PheGenIrs13015955
hapmaprs13015955
1000 genomesrs13015955
hgdprs13015955
ensemblrs13015955
gopubmedrs13015955
geneviewrs13015955
scholarrs13015955
googlers13015955
pharmgkbrs13015955
gwascentralrs13015955
openSNPrs13015955
23andMers13015955
23andMe allrs13015955
SNP Nexus

SNPshotrs13015955
SNPdbers13015955
MSV3drs13015955
GWAS Ctlgrs13015955
GMAF0.1185
Max Magnitude
? (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 4E-7
Odds Ratio 0.1790 [0.11-0.25] SD increase