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rs11661542

From SNPedia

Orientationplus
Stabilizedplus
Make rs11661542(A;A)
Make rs11661542(A;C)
Make rs11661542(C;C)
ReferenceGRCh38 38.1/141
Chromosome18
Position22643732
is asnp
is mentioned by
dbSNPrs11661542
ebirs11661542
HLIrs11661542
Exacrs11661542
Varsomers11661542
Maprs11661542
PheGenIrs11661542
hapmaprs11661542
1000 genomesrs11661542
hgdprs11661542
ensemblrs11661542
gopubmedrs11661542
geneviewrs11661542
scholarrs11661542
googlers11661542
pharmgkbrs11661542
gwascentralrs11661542
openSNPrs11661542
23andMers11661542
23andMe allrs11661542
SNP Nexus

SNPshotrs11661542
SNPdbers11661542
MSV3drs11661542
GWAS Ctlgrs11661542
GMAF0.3646
Max Magnitude
? (A;A) (A;C) (C;C) 28

Based on a large study (~6,000 cases and 14,000 controls) of both European and Japanese populations, the rs11661542(C) allele has been associated with higher risk of aneurysm, with an odds ratio per allele of 1.22 (CI: 1.15-1.28, p=1.1e-12). [PMID 20364137OA-icon.png]

OMIM105800
Desc
Variant
Relatedalso