rs63749932(T;T)
From SNPedia
| Lynch syndrome; hereditary nonpolyposis colorectal cancer (HNPCC1) |
| Is a | genotype |
| of | rs63749932 |
| Gene | MSH2 |
| Chromosome | 2 |
| Position | 47,476,399 |
| mentioned | by |
| Magnitude | 6 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| (C;T) | 6 | Lynch syndrome; pathogenic mutation |
| (T;T) | 6 | Lynch syndrome; hereditary nonpolyposis colorectal cancer (HNPCC1) |
Lynch syndrome; hereditary nonpolyposis colorectal cancer (HNPCC1)
