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rs2346177

From SNPedia

Orientationplus
Stabilizedplus
Make rs2346177(A;A)
Make rs2346177(A;G)
Make rs2346177(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position46415110
is asnp
is mentioned by
dbSNPrs2346177
ebirs2346177
HLIrs2346177
Exacrs2346177
Varsomers2346177
Maprs2346177
PheGenIrs2346177
hapmaprs2346177
1000 genomesrs2346177
hgdprs2346177
ensemblrs2346177
gopubmedrs2346177
geneviewrs2346177
scholarrs2346177
googlers2346177
pharmgkbrs2346177
gwascentralrs2346177
openSNPrs2346177
23andMers2346177
23andMe allrs2346177
SNP Nexus

SNPshotrs2346177
SNPdbers2346177
MSV3drs2346177
GWAS Ctlgrs2346177
GMAF0.4715
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 0.000002
Odds Ratio 0.0728 [0.04-0.10] SD increase