rs587776771
From SNPedia
Orientation | plus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
(CT;CT) | 0 | common in clinvar |
(G;G) | 0 | common in clinvar |
(I;I) | 0 | common genotype |
Make rs587776771(-;-) |
Make rs587776771(-;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 17 |
Position | 37744839 |
Gene | HNF1B |
is a | snp |
is | mentioned by |
dbSNP | rs587776771 |
dbSNP (classic) | rs587776771 |
ClinGen | rs587776771 |
ebi | rs587776771 |
HLI | rs587776771 |
Exac | rs587776771 |
Gnomad | rs587776771 |
Varsome | rs587776771 |
LitVar | rs587776771 |
Map | rs587776771 |
PheGenI | rs587776771 |
Biobank | rs587776771 |
1000 genomes | rs587776771 |
hgdp | rs587776771 |
ensembl | rs587776771 |
geneview | rs587776771 |
scholar | rs587776771 |
rs587776771 | |
pharmgkb | rs587776771 |
gwascentral | rs587776771 |
openSNP | rs587776771 |
23andMe | rs587776771 |
SNPshot | rs587776771 |
SNPdbe | rs587776771 |
MSV3d | rs587776771 |
GWAS Ctlg | rs587776771 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | Rs587776771(G;G) rs587776771(-;-) |
Alt | Rs587776771(G;G) rs587776771(-;-) |
Reference | Rs587776771(C;C) |
Significance | Pathogenic |
Disease | Chromophobe renal cell carcinoma |
Variation | info |
Gene | HNF1B |
CLNDBN | Chromophobe renal cell carcinoma |
Reversed | 1 |
HGVS | NC_000017.10:g.36104830delG |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000013483.23, |