rs138775799
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs138775799(A;A) |
| Make rs138775799(A;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 1 |
| Position | 45333472 |
| Gene | MUTYH |
| is a | snp |
| is | mentioned by |
| dbSNP | rs138775799 |
| dbSNP (classic) | rs138775799 |
| ClinGen | rs138775799 |
| ebi | rs138775799 |
| HLI | rs138775799 |
| Exac | rs138775799 |
| Gnomad | rs138775799 |
| Varsome | rs138775799 |
| LitVar | rs138775799 |
| Map | rs138775799 |
| PheGenI | rs138775799 |
| Biobank | rs138775799 |
| 1000 genomes | rs138775799 |
| hgdp | rs138775799 |
| ensembl | rs138775799 |
| geneview | rs138775799 |
| scholar | rs138775799 |
| rs138775799 | |
| pharmgkb | rs138775799 |
| gwascentral | rs138775799 |
| openSNP | rs138775799 |
| 23andMe | rs138775799 |
| SNPshot | rs138775799 |
| SNPdbe | rs138775799 |
| MSV3d | rs138775799 |
| GWAS Ctlg | rs138775799 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs138775799(A;A) |
| Alt | rs138775799(A;A) |
| Reference | Rs138775799(G;G) |
| 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 | 0 |
| HGVS | NC_000001.10:g.45799144G>A |
| CLNSRC | Ambry Genetics ClinVar |
| CLNACC | RCV000129018.3, RCV000235267.1, RCV000471769.1, |
