rs587776705(-;GTG)
From SNPedia
| Variant of uncertain significance; possible Lynch syndrome mutation |
| Is a | genotype |
| of | rs587776705 |
| Gene | MSH6 |
| Chromosome | 2 |
| Position | 47,803,633 |
| mentioned | by |
| Magnitude | 5 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (-;GTG) | 5 | Variant of uncertain significance; possible Lynch syndrome mutation |
| (GTG;GTG) | 0 | common in clinvar |
Listed in ClinVar as being of uncertain significance, the minor allele of this genotype, causing an in-frame deletion, may be linked to certain cancers, but it has not been proven to be causative.
