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rs1475591

From SNPedia

Orientationplus
Stabilizedplus
Make rs1475591(C;C)
Make rs1475591(C;T)
Make rs1475591(T;T)
ReferenceGRCh38 38.1/141
Chromosome21
Position31068221
is asnp
is mentioned by
dbSNPrs1475591
ebirs1475591
HLIrs1475591
Exacrs1475591
Varsomers1475591
Maprs1475591
PheGenIrs1475591
hapmaprs1475591
1000 genomesrs1475591
hgdprs1475591
ensemblrs1475591
gopubmedrs1475591
geneviewrs1475591
scholarrs1475591
googlers1475591
pharmgkbrs1475591
gwascentralrs1475591
openSNPrs1475591
23andMers1475591
23andMe allrs1475591
SNP Nexus

SNPshotrs1475591
SNPdbers1475591
MSV3drs1475591
GWAS Ctlgrs1475591
GMAF0.1478
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 0.000006
Odds Ratio 1.1800 [1.10-1.27]