rs886041689
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Chromosome | 17 |
| Position | 37733556 |
| Gene | HNF1B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs886041689 |
| dbSNP (classic) | rs886041689 |
| ClinGen | rs886041689 |
| ebi | rs886041689 |
| HLI | rs886041689 |
| Exac | rs886041689 |
| Gnomad | rs886041689 |
| Varsome | rs886041689 |
| LitVar | rs886041689 |
| Map | rs886041689 |
| PheGenI | rs886041689 |
| Biobank | rs886041689 |
| 1000 genomes | rs886041689 |
| hgdp | rs886041689 |
| ensembl | rs886041689 |
| geneview | rs886041689 |
| scholar | rs886041689 |
| rs886041689 | |
| pharmgkb | rs886041689 |
| gwascentral | rs886041689 |
| openSNP | rs886041689 |
| 23andMe | rs886041689 |
| SNPshot | rs886041689 |
| SNPdbe | rs886041689 |
| MSV3d | rs886041689 |
| GWAS Ctlg | rs886041689 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs886041689(T;T) |
| Alt | rs886041689(T;T) |
| Reference | Rs886041689(G;G) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | HNF1B |
| CLNDBN | not provided |
| Reversed | 1 |
| HGVS | NC_000017.10:g.36093549C>A |
| CLNSRC | |
| CLNACC | RCV000265224.1, |
