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rs17577085

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs17577085(G;G)
Make rs17577085(G;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position142484039
is asnp
is mentioned by
dbSNPrs17577085
ebirs17577085
HLIrs17577085
Exacrs17577085
Varsomers17577085
Maprs17577085
PheGenIrs17577085
hapmaprs17577085
1000 genomesrs17577085
hgdprs17577085
ensemblrs17577085
gopubmedrs17577085
geneviewrs17577085
scholarrs17577085
googlers17577085
pharmgkbrs17577085
gwascentralrs17577085
openSNPrs17577085
23andMers17577085
23andMe allrs17577085
SNP Nexus

SNPshotrs17577085
SNPdbers17577085
MSV3drs17577085
GWAS Ctlgrs17577085
GMAF0.05877
Max Magnitude0
? (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
P-val 0.000004
Odds Ratio 2.6300 [1.72-3.85]