rs10788165
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10788165(G;G) |
Make rs10788165(G;T) |
Make rs10788165(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 121284700 |
is a | snp |
is | mentioned by |
dbSNP | rs10788165 |
dbSNP (classic) | rs10788165 |
ClinGen | rs10788165 |
ebi | rs10788165 |
HLI | rs10788165 |
Exac | rs10788165 |
Gnomad | rs10788165 |
Varsome | rs10788165 |
LitVar | rs10788165 |
Map | rs10788165 |
PheGenI | rs10788165 |
Biobank | rs10788165 |
1000 genomes | rs10788165 |
hgdp | rs10788165 |
ensembl | rs10788165 |
geneview | rs10788165 |
scholar | rs10788165 |
rs10788165 | |
pharmgkb | rs10788165 |
gwascentral | rs10788165 |
openSNP | rs10788165 |
23andMe | rs10788165 |
SNPshot | rs10788165 |
SNPdbe | rs10788165 |
MSV3d | rs10788165 |
GWAS Ctlg | rs10788165 |
GMAF | 0.3347 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
[PMID 22130093] New variants at 10q26 and 15q21 are associated with aggressive prostate cancer in a genome-wide association study from a prostate biopsy screening cohort
[PMID 20514297] 2010 CUA Abstracts.
[PMID 22523086] Gene variants in the angiogenesis pathway and prostate cancer.