rs11199874
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11199874(A;A) |
Make rs11199874(A;G) |
Make rs11199874(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 121273005 |
is a | snp |
is | mentioned by |
dbSNP | rs11199874 |
dbSNP (classic) | rs11199874 |
ClinGen | rs11199874 |
ebi | rs11199874 |
HLI | rs11199874 |
Exac | rs11199874 |
Gnomad | rs11199874 |
Varsome | rs11199874 |
LitVar | rs11199874 |
Map | rs11199874 |
PheGenI | rs11199874 |
Biobank | rs11199874 |
1000 genomes | rs11199874 |
hgdp | rs11199874 |
ensembl | rs11199874 |
geneview | rs11199874 |
scholar | rs11199874 |
rs11199874 | |
pharmgkb | rs11199874 |
gwascentral | rs11199874 |
openSNP | rs11199874 |
23andMe | rs11199874 |
SNPshot | rs11199874 |
SNPdbe | rs11199874 |
MSV3d | rs11199874 |
GWAS Ctlg | rs11199874 |
GMAF | 0.214 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22130093] |
Trait | |
Title | New variants at 10q26 and 15q21 are associated with aggressive prostate cancer in a genome-wide association study from a prostate biopsy screening cohort. |
Risk Allele | |
P-val | 3E-10 |
Odds Ratio | None None |
[PMID 22523086] Gene variants in the angiogenesis pathway and prostate cancer.