rs267607883
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Make rs267607883(A;G) |
| Make rs267607883(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 37048902 |
| Gene | MLH1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs267607883 |
| ClinGen | rs267607883 |
| ebi | rs267607883 |
| HLI | rs267607883 |
| Exac | rs267607883 |
| Varsome | rs267607883 |
| Map | rs267607883 |
| PheGenI | rs267607883 |
| hapmap | rs267607883 |
| 1000 genomes | rs267607883 |
| hgdp | rs267607883 |
| ensembl | rs267607883 |
| gopubmed | rs267607883 |
| geneview | rs267607883 |
| scholar | rs267607883 |
| rs267607883 | |
| pharmgkb | rs267607883 |
| gwascentral | rs267607883 |
| openSNP | rs267607883 |
| 23andMe | rs267607883 |
| 23andMe all | rs267607883 |
| SNP Nexus | |
| SNPshot | rs267607883 |
| SNPdbe | rs267607883 |
| MSV3d | rs267607883 |
| GWAS Ctlg | rs267607883 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs267607883(G;G) |
| Alt | rs267607883(G;G) |
| Reference | Rs267607883(A;A) |
| Significance | Pathogenic |
| Disease | Lynch syndrome not provided |
| Variation | info |
| Gene | MLH1 |
| CLNDBN | Lynch syndrome not provided |
| Reversed | 0 |
| HGVS | NC_000003.11:g.37090393A>G |
| CLNSRC | International Society for Gastrointestinal Hereditary Tumours |
| CLNACC | RCV000075469.2, RCV000202242.1, |
