rs2346177

Orientation

plus

Stabilized

plus

Make rs2346177(A;A)

Make rs2346177(A;G)

Make rs2346177(G;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

46415110

is a	snp
is	mentioned by
dbSNP	rs2346177
dbSNP (classic)	rs2346177
ClinGen	rs2346177
ebi	rs2346177
HLI	rs2346177
Exac	rs2346177
Gnomad	rs2346177
Varsome	rs2346177
LitVar	rs2346177
Map	rs2346177
PheGenI	rs2346177
Biobank	rs2346177
1000 genomes	rs2346177
hgdp	rs2346177
ensembl	rs2346177
geneview	rs2346177
scholar	rs2346177
google	rs2346177
pharmgkb	rs2346177
gwascentral	rs2346177
openSNP	rs2346177
23andMe	rs2346177
SNPshot	rs2346177
SNPdbe	rs2346177
MSV3d	rs2346177
GWAS Ctlg	rs2346177

GMAF

0.4715

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

GWAS snp
PMID	[PMID 21347282]
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