rs11661542
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11661542(A;A) |
Make rs11661542(A;C) |
Make rs11661542(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 18 |
Position | 22643732 |
is a | snp |
is | mentioned by |
dbSNP | rs11661542 |
dbSNP (classic) | rs11661542 |
ClinGen | rs11661542 |
ebi | rs11661542 |
HLI | rs11661542 |
Exac | rs11661542 |
Gnomad | rs11661542 |
Varsome | rs11661542 |
LitVar | rs11661542 |
Map | rs11661542 |
PheGenI | rs11661542 |
Biobank | rs11661542 |
1000 genomes | rs11661542 |
hgdp | rs11661542 |
ensembl | rs11661542 |
geneview | rs11661542 |
scholar | rs11661542 |
rs11661542 | |
pharmgkb | rs11661542 |
gwascentral | rs11661542 |
openSNP | rs11661542 |
23andMe | rs11661542 |
SNPshot | rs11661542 |
SNPdbe | rs11661542 |
MSV3d | rs11661542 |
GWAS Ctlg | rs11661542 |
GMAF | 0.3646 |
Max Magnitude | 0 |
? | (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 20364137]