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rs63749942(GTC;GTC)

From SNPedia
common in clinvar
Is agenotype
ofrs63749942
GeneMSH6
Chromosome2
Position47,806,281
Merged fromRs587781362
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;CGT) 6 Lynch syndrome, pathogenic mutation
(CGT;CGT) 0 common in clinvar
(GTC;GTC) 0 common in clinvar
(I;I) 0