Have questions? Visit https://www.reddit.com/r/SNPedia

rs744487

From SNPedia

Orientationminus
Stabilizedminus
Make rs744487(G;G)
Make rs744487(G;T)
Make rs744487(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position234590266
is asnp
is mentioned by
dbSNPrs744487
ebirs744487
HLIrs744487
Exacrs744487
Varsomers744487
Maprs744487
PheGenIrs744487
hapmaprs744487
1000 genomesrs744487
hgdprs744487
ensemblrs744487
gopubmedrs744487
geneviewrs744487
scholarrs744487
googlers744487
pharmgkbrs744487
gwascentralrs744487
openSNPrs744487
23andMers744487
23andMe allrs744487
SNP Nexus

SNPshotrs744487
SNPdbers744487
MSV3drs744487
GWAS Ctlgrs744487
GMAF0.2746
Max Magnitude
? (G;G) (G;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 0.000005
Odds Ratio 0.0690 [0.04-0.10] SD decrease