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

rs17589290

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs17589290(C;G)
Make rs17589290(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position112002081
is asnp
is mentioned by
dbSNPrs17589290
ebirs17589290
HLIrs17589290
Exacrs17589290
Varsomers17589290
Maprs17589290
PheGenIrs17589290
hapmaprs17589290
1000 genomesrs17589290
hgdprs17589290
ensemblrs17589290
gopubmedrs17589290
geneviewrs17589290
scholarrs17589290
googlers17589290
pharmgkbrs17589290
gwascentralrs17589290
openSNPrs17589290
23andMers17589290
23andMe allrs17589290
SNP Nexus

SNPshotrs17589290
SNPdbers17589290
MSV3drs17589290
GWAS Ctlgrs17589290
GMAF0.05969
Max Magnitude0
? (C;C) (C;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
P-val 0.000006
Odds Ratio 1.4300 [1.22-1.67]