rs63750714(-;C)
From SNPedia
Unclear significance; possible Lynch syndrome mutation |
Is a | genotype |
of | rs63750714 |
Gene | MSH6 |
Chromosome | 2 |
Position | 47,803,442 |
mentioned | by |
Magnitude | 5 |
Repute | Bad |
Geno | Mag | Summary |
---|---|---|
(-;C) | 5 | Unclear significance; possible Lynch syndrome mutation |
(C;C) | 0 | common/normal |
This mutation is not listed in ClinVar, but as in frameshift mutation in the MSH6 gene, it appears likely to be as problematic as similar neighbouring mutations. Anyone with information about the pathogenicity of this mutation is encouraged to contact us.