rs2005705
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2005705(C;C) |
Make rs2005705(C;T) |
Make rs2005705(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 17 |
Position | 37736310 |
Gene | HNF1B |
is a | snp |
is | mentioned by |
dbSNP | rs2005705 |
dbSNP (classic) | rs2005705 |
ClinGen | rs2005705 |
ebi | rs2005705 |
HLI | rs2005705 |
Exac | rs2005705 |
Gnomad | rs2005705 |
Varsome | rs2005705 |
LitVar | rs2005705 |
Map | rs2005705 |
PheGenI | rs2005705 |
Biobank | rs2005705 |
1000 genomes | rs2005705 |
hgdp | rs2005705 |
ensembl | rs2005705 |
geneview | rs2005705 |
scholar | rs2005705 |
rs2005705 | |
pharmgkb | rs2005705 |
gwascentral | rs2005705 |
openSNP | rs2005705 |
23andMe | rs2005705 |
SNPshot | rs2005705 |
SNPdbe | rs2005705 |
MSV3d | rs2005705 |
GWAS Ctlg | rs2005705 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 24740154] |
Trait | Prostate cancer (early onset) |
Title | Genome-wide association scan for variants associated with early-onset prostate cancer. |
Risk Allele | G |
P-val | 1E-6 |
Odds Ratio | 1.35 [1.23-1.47] |