rs10502575

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common genotype

Make rs10502575(A;G)

Make rs10502575(G;G)

Reference

GRCh38 38.1/141

Chromosome

18

Position

31756628

is a	snp
is	mentioned by
dbSNP	rs10502575
dbSNP (classic)	rs10502575
ClinGen	rs10502575
ebi	rs10502575
HLI	rs10502575
Exac	rs10502575
Gnomad	rs10502575
Varsome	rs10502575
LitVar	rs10502575
Map	rs10502575
PheGenI	rs10502575
Biobank	rs10502575
1000 genomes	rs10502575
hgdp	rs10502575
ensembl	rs10502575
geneview	rs10502575
scholar	rs10502575
google	rs10502575
pharmgkb	rs10502575
gwascentral	rs10502575
openSNP	rs10502575
23andMe	rs10502575
SNPshot	rs10502575
SNPdbe	rs10502575
MSV3d	rs10502575
GWAS Ctlg	rs10502575

GMAF

0.04454

Max Magnitude

0

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

GWAS snp
PMID	[PMID 23870195]
Trait	Coronary artery calcification
Title	Genetics of coronary artery calcification among African Americans, a meta-analysis.
Risk Allele	A
P-val	1E-7
Odds Ratio	.22 [0.14-0.3] unit increase