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rs11053646

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs11053646(C;G)
Make rs11053646(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position10160849
GeneOLR1
is asnp
is mentioned by
dbSNPrs11053646
ebirs11053646
HLIrs11053646
Exacrs11053646
Varsomers11053646
Maprs11053646
PheGenIrs11053646
hapmaprs11053646
1000 genomesrs11053646
hgdprs11053646
ensemblrs11053646
gopubmedrs11053646
geneviewrs11053646
scholarrs11053646
googlers11053646
pharmgkbrs11053646
gwascentralrs11053646
openSNPrs11053646
23andMers11053646
23andMe allrs11053646
SNP Nexus

SNPshotrs11053646
SNPdbers11053646
MSV3drs11053646
GWAS Ctlgrs11053646
GMAF0.1322
Max Magnitude0
? (C;C) (C;G) (G;G) 28
OMIM602601
DescMYOCARDIAL INFARCTION, SUSCEPTIBILITY TO
Variant0002
Relatedalso


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

[PMID 21257822OA-icon.png] 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
CLNACC RCV000007409.2,



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


GET Evidence
OLR1-K167N
aa_change Lys167Asn
aa_change_short K167N
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.13404
summary



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


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