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rs63750714(-;C)

From SNPedia
Unclear significance; possible Lynch syndrome mutation
Is agenotype
ofrs63750714
GeneMSH6
Chromosome2
Position47,803,442
mentionedby
Magnitude5
ReputeBad
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.