rs1016990
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1016990(C;C) |
Make rs1016990(C;G) |
Make rs1016990(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 37728924 |
Gene | HNF1B |
is a | snp |
is | mentioned by |
dbSNP | rs1016990 |
dbSNP (classic) | rs1016990 |
ClinGen | rs1016990 |
ebi | rs1016990 |
HLI | rs1016990 |
Exac | rs1016990 |
Gnomad | rs1016990 |
Varsome | rs1016990 |
LitVar | rs1016990 |
Map | rs1016990 |
PheGenI | rs1016990 |
Biobank | rs1016990 |
1000 genomes | rs1016990 |
hgdp | rs1016990 |
ensembl | rs1016990 |
geneview | rs1016990 |
scholar | rs1016990 |
rs1016990 | |
pharmgkb | rs1016990 |
gwascentral | rs1016990 |
openSNP | rs1016990 |
23andMe | rs1016990 |
SNPshot | rs1016990 |
SNPdbe | rs1016990 |
MSV3d | rs1016990 |
GWAS Ctlg | rs1016990 |
GMAF | 0.2686 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 21576123] Large-scale fine mapping of the HNF1B locus and prostate cancer risk [PMID 19168595] Common variants of hepatocyte nuclear factor 1beta are associated with type 2 diabetes in a Chinese population.