rs10749408
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10749408(C;C) |
Make rs10749408(C;T) |
Make rs10749408(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 121208012 |
is a | snp |
is | mentioned by |
dbSNP | rs10749408 |
dbSNP (classic) | rs10749408 |
ClinGen | rs10749408 |
ebi | rs10749408 |
HLI | rs10749408 |
Exac | rs10749408 |
Gnomad | rs10749408 |
Varsome | rs10749408 |
LitVar | rs10749408 |
Map | rs10749408 |
PheGenI | rs10749408 |
Biobank | rs10749408 |
1000 genomes | rs10749408 |
hgdp | rs10749408 |
ensembl | rs10749408 |
geneview | rs10749408 |
scholar | rs10749408 |
rs10749408 | |
pharmgkb | rs10749408 |
gwascentral | rs10749408 |
openSNP | rs10749408 |
23andMe | rs10749408 |
SNPshot | rs10749408 |
SNPdbe | rs10749408 |
MSV3d | rs10749408 |
GWAS Ctlg | rs10749408 |
GMAF | 0.2585 |
Max Magnitude | 0 |
? | (C;C) (C;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.