rs113042313
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs113042313(C;T) |
| Make rs113042313(T;T) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 17 |
| Position | 37710601 |
| Gene | HNF1B, LOC105371754 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs113042313 |
| dbSNP (classic) | rs113042313 |
| ClinGen | rs113042313 |
| ebi | rs113042313 |
| HLI | rs113042313 |
| Exac | rs113042313 |
| Gnomad | rs113042313 |
| Varsome | rs113042313 |
| LitVar | rs113042313 |
| Map | rs113042313 |
| PheGenI | rs113042313 |
| Biobank | rs113042313 |
| 1000 genomes | rs113042313 |
| hgdp | rs113042313 |
| ensembl | rs113042313 |
| geneview | rs113042313 |
| scholar | rs113042313 |
| rs113042313 | |
| pharmgkb | rs113042313 |
| gwascentral | rs113042313 |
| openSNP | rs113042313 |
| 23andMe | rs113042313 |
| SNPshot | rs113042313 |
| SNPdbe | rs113042313 |
| MSV3d | rs113042313 |
| GWAS Ctlg | rs113042313 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs113042313(T;T) |
| Alt | rs113042313(T;T) |
| Reference | Rs113042313(C;C) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | HNF1B |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000017.10:g.36070609C>T |
| CLNSRC | |
| CLNACC | RCV000429473.1, |
