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rs587776705(-;GTG)

From SNPedia
(Redirected from I5901124(D;I))
Variant of uncertain significance; possible Lynch syndrome mutation
Is agenotype
ofrs587776705
GeneMSH6
Chromosome2
Position47,803,633
mentionedby
Magnitude5
ReputeBad
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.