| common in clinvar |
| Is a | genotype |
| of | rs267608120 |
| Gene | MSH6, FBXO11 |
| Chromosome | 2 |
| Position | 47,806,609 |
| Merged from | Rs267608119 |
| mentioned | by |
| Magnitude | 0 |
| Repute | Good |
| Geno | Mag | Summary |
|---|---|---|
| (-;CAAG) | 6 | Lynch syndrome, pathogenic mutation |
| (AAGC;AAGC) | 0 | common in clinvar |
| (CAAG;CAAG) | 0 | common in clinvar |
