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rs63749938(A;A)

From SNPedia
common in clinvar
Is agenotype
ofrs63749938
GeneMSH6
Chromosome2
Position47,800,967
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;A) 6 Lynch Syndrome, pathogenic mutation
(A;A) 0 common in clinvar
(I;I) 0