rs2074429
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2074429(A;A) |
Make rs2074429(A;G) |
Make rs2074429(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 37701292 |
Gene | HNF1B |
is a | snp |
is | mentioned by |
dbSNP | rs2074429 |
dbSNP (classic) | rs2074429 |
ClinGen | rs2074429 |
ebi | rs2074429 |
HLI | rs2074429 |
Exac | rs2074429 |
Gnomad | rs2074429 |
Varsome | rs2074429 |
LitVar | rs2074429 |
Map | rs2074429 |
PheGenI | rs2074429 |
Biobank | rs2074429 |
1000 genomes | rs2074429 |
hgdp | rs2074429 |
ensembl | rs2074429 |
geneview | rs2074429 |
scholar | rs2074429 |
rs2074429 | |
pharmgkb | rs2074429 |
gwascentral | rs2074429 |
openSNP | rs2074429 |
23andMe | rs2074429 |
SNPshot | rs2074429 |
SNPdbe | rs2074429 |
MSV3d | rs2074429 |
GWAS Ctlg | rs2074429 |
GMAF | 0.2195 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 21982019] HNF1B Polymorphism Associated With Development of Prostate Cancer in Korean Patients