rs13424957

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in complete genomics

Make rs13424957(C;T)

Make rs13424957(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

164893880

Gene	LOC101929633

is a	snp
is	mentioned by
dbSNP	rs13424957
dbSNP (classic)	rs13424957
ClinGen	rs13424957
ebi	rs13424957
HLI	rs13424957
Exac	rs13424957
Gnomad	rs13424957
Varsome	rs13424957
LitVar	rs13424957
Map	rs13424957
PheGenI	rs13424957
Biobank	rs13424957
1000 genomes	rs13424957
hgdp	rs13424957
ensembl	rs13424957
geneview	rs13424957
scholar	rs13424957
google	rs13424957
pharmgkb	rs13424957
gwascentral	rs13424957
openSNP	rs13424957
23andMe	rs13424957
SNPshot	rs13424957
SNPdbe	rs13424957
MSV3d	rs13424957
GWAS Ctlg	rs13424957

GMAF

0.05693

Max Magnitude

0

?	(C;C) (C;T) (T;T)	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
P-val	0.000003
Odds Ratio	1.2400 [1.14-1.36]