rs11650066
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11650066(A;A) |
Make rs11650066(A;G) |
Make rs11650066(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 33960430 |
Gene | ASIC2, LOC107985038 |
is a | snp |
is | mentioned by |
dbSNP | rs11650066 |
dbSNP (classic) | rs11650066 |
ClinGen | rs11650066 |
ebi | rs11650066 |
HLI | rs11650066 |
Exac | rs11650066 |
Gnomad | rs11650066 |
Varsome | rs11650066 |
LitVar | rs11650066 |
Map | rs11650066 |
PheGenI | rs11650066 |
Biobank | rs11650066 |
1000 genomes | rs11650066 |
hgdp | rs11650066 |
ensembl | rs11650066 |
geneview | rs11650066 |
scholar | rs11650066 |
rs11650066 | |
pharmgkb | rs11650066 |
gwascentral | rs11650066 |
openSNP | rs11650066 |
23andMe | rs11650066 |
SNPshot | rs11650066 |
SNPdbe | rs11650066 |
MSV3d | rs11650066 |
GWAS Ctlg | rs11650066 |
GMAF | 0.3017 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21378988] |
Trait | |
Title | A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease |
Risk Allele | |
P-val | 0.000006 |
Odds Ratio | None None |