rs267608149
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (-;-) | 0 | common in clinvar |
| (-;T) | 6 | Lynch syndrome, pathogenic mutation |
| Make rs267608149(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 5997326 |
| Gene | PMS2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs267608149 |
| dbSNP (classic) | rs267608149 |
| ClinGen | rs267608149 |
| ebi | rs267608149 |
| HLI | rs267608149 |
| Exac | rs267608149 |
| Gnomad | rs267608149 |
| Varsome | rs267608149 |
| LitVar | rs267608149 |
| Map | rs267608149 |
| PheGenI | rs267608149 |
| Biobank | rs267608149 |
| 1000 genomes | rs267608149 |
| hgdp | rs267608149 |
| ensembl | rs267608149 |
| geneview | rs267608149 |
| scholar | rs267608149 |
| rs267608149 | |
| pharmgkb | rs267608149 |
| gwascentral | rs267608149 |
| openSNP | rs267608149 |
| 23andMe | rs267608149 |
| SNPshot | rs267608149 |
| SNPdbe | rs267608149 |
| MSV3d | rs267608149 |
| GWAS Ctlg | rs267608149 |
| Max Magnitude | 6 |
| ClinVar | |
|---|---|
| Risk | rs267608149(T;T) |
| Alt | rs267608149(T;T) |
| Reference | Rs267608149(-;-) |
| Significance | Pathogenic |
| Disease | Lynch syndrome |
| Variation | info |
| Gene | PMS2 |
| CLNDBN | Lynch syndrome |
| Reversed | 1 |
| HGVS | NC_000007.13:g.6036958dupA |
| CLNSRC | International Society for Gastrointestinal Hereditary Tumours |
| CLNACC | RCV000076888.2, |
