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rs63750039(T;T)

From SNPedia
common in clinvar
Is agenotype
ofrs63750039
GeneMSH2
Chromosome2
Position47,429,804
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;T) 6 Lynch syndrome, pathogenic mutation
(I;I) 0
(T;T) 0 common in clinvar