rs34126013
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs34126013(C;T) |
| Make rs34126013(T;T) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 1 |
| Position | 45332458 |
| Gene | MUTYH |
| is a | snp |
| is | mentioned by |
| dbSNP | rs34126013 |
| dbSNP (classic) | rs34126013 |
| ClinGen | rs34126013 |
| ebi | rs34126013 |
| HLI | rs34126013 |
| Exac | rs34126013 |
| Gnomad | rs34126013 |
| Varsome | rs34126013 |
| LitVar | rs34126013 |
| Map | rs34126013 |
| PheGenI | rs34126013 |
| Biobank | rs34126013 |
| 1000 genomes | rs34126013 |
| hgdp | rs34126013 |
| ensembl | rs34126013 |
| geneview | rs34126013 |
| scholar | rs34126013 |
| rs34126013 | |
| pharmgkb | rs34126013 |
| gwascentral | rs34126013 |
| openSNP | rs34126013 |
| 23andMe | rs34126013 |
| SNPshot | rs34126013 |
| SNPdbe | rs34126013 |
| MSV3d | rs34126013 |
| GWAS Ctlg | rs34126013 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs34126013(T;T) |
| Alt | rs34126013(T;T) |
| Reference | Rs34126013(C;C) |
| Significance | Pathogenic |
| Disease | Hereditary cancer-predisposing syndrome not provided MYH-associated polyposis |
| Variation | info |
| Gene | MUTYH |
| CLNDBN | Hereditary cancer-predisposing syndrome not provided MYH-associated polyposis |
| Reversed | 1 |
| HGVS | NC_000001.10:g.45798130G>A |
| CLNSRC | |
| CLNACC | RCV000164664.3, RCV000235834.1, RCV000369240.1, |
