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rs63749821(-;-)

From SNPedia
common in clinvar
Is agenotype
ofrs63749821
GeneMSH6
Chromosome2
Position47,803,446
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;-) 0 common in clinvar
(-;TA) 6 Likely miscall in Ancestry data; otherwise, Lynch syndrome, pathogenic mutation
(I;I) 0