rs11053646

Orientation

plus

Stabilized

plus

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

Make rs11053646(C;G)

Make rs11053646(G;G)

Reference

GRCh38 38.1/141

Chromosome

12

Position

10160849

Gene

OLR1

is a	snp
is	mentioned by
dbSNP	rs11053646
dbSNP (classic)	rs11053646
ClinGen	rs11053646
ebi	rs11053646
HLI	rs11053646
Exac	rs11053646
Gnomad	rs11053646
Varsome	rs11053646
LitVar	rs11053646
Map	rs11053646
PheGenI	rs11053646
Biobank	rs11053646
1000 genomes	rs11053646
hgdp	rs11053646
ensembl	rs11053646
geneview	rs11053646
scholar	rs11053646
google	rs11053646
pharmgkb	rs11053646
gwascentral	rs11053646
openSNP	rs11053646
23andMe	rs11053646
SNPshot	rs11053646
SNPdbe	rs11053646
MSV3d	rs11053646
GWAS Ctlg	rs11053646

GMAF

0.1322

Max Magnitude

0

?	(C;C) (C;G) (G;G)	28

OMIM	602601
Desc	MYOCARDIAL INFARCTION, SUSCEPTIBILITY TO
Variant	0002
Related	also

[PMID 19961348] Population differences in allele frequencies at the OLR1 locus may suggest geographic disparities in cardiovascular risk events

[PMID 21257822] A Candidate Gene Study Revealed Sex-Specific Association Between the OLR1 Gene and Carotid Plaque

ClinVar
Risk	rs11053646(G;G)
Alt	rs11053646(G;G)
Reference	Rs11053646(C;C)
Significance	Other
Disease	Myocardial infarction
Variation	info
Gene	OLR1
CLNDBN	Myocardial infarction
Reversed	0
HGVS	NC_000012.11:g.10313448C>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000007409.2,

[PMID 18384690] Failure to replicate an association of SNPs in the oxidized LDL receptor gene (OLR1) with CAD.

[PMID 23535804] The role of OLR1 polymorphisms in determining the risk and prognosis of ischemic stroke in a Chinese population

[PMID 23274712] Genetic polymorphisms and the risk of myocardial infarction in patients under 45 years of age.