rs9567349
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in complete genomics |
Make rs9567349(A;G) |
Make rs9567349(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 44063269 |
is a | snp |
is | mentioned by |
dbSNP | rs9567349 |
dbSNP (classic) | rs9567349 |
ClinGen | rs9567349 |
ebi | rs9567349 |
HLI | rs9567349 |
Exac | rs9567349 |
Gnomad | rs9567349 |
Varsome | rs9567349 |
LitVar | rs9567349 |
Map | rs9567349 |
PheGenI | rs9567349 |
Biobank | rs9567349 |
1000 genomes | rs9567349 |
hgdp | rs9567349 |
ensembl | rs9567349 |
geneview | rs9567349 |
scholar | rs9567349 |
rs9567349 | |
pharmgkb | rs9567349 |
gwascentral | rs9567349 |
openSNP | rs9567349 |
23andMe | rs9567349 |
SNPshot | rs9567349 |
SNPdbe | rs9567349 |
MSV3d | rs9567349 |
GWAS Ctlg | rs9567349 |
GMAF | 0.1621 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22219177] |
Trait | |
Title | A genome-wide search for loci interacting with known prostate cancer risk-associated genetic variants. |
Risk Allele | |
P-val | 0.000004 |
Odds Ratio | 1.6393 None |