rs11263763
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11263763(A;A) |
Make rs11263763(A;G) |
Make rs11263763(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 17 |
Position | 37743574 |
Gene | HNF1B |
is a | snp |
is | mentioned by |
dbSNP | rs11263763 |
dbSNP (classic) | rs11263763 |
ClinGen | rs11263763 |
ebi | rs11263763 |
HLI | rs11263763 |
Exac | rs11263763 |
Gnomad | rs11263763 |
Varsome | rs11263763 |
LitVar | rs11263763 |
Map | rs11263763 |
PheGenI | rs11263763 |
Biobank | rs11263763 |
1000 genomes | rs11263763 |
hgdp | rs11263763 |
ensembl | rs11263763 |
geneview | rs11263763 |
scholar | rs11263763 |
rs11263763 | |
pharmgkb | rs11263763 |
gwascentral | rs11263763 |
openSNP | rs11263763 |
23andMe | rs11263763 |
SNPshot | rs11263763 |
SNPdbe | rs11263763 |
MSV3d | rs11263763 |
GWAS Ctlg | rs11263763 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 25378557] Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk