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rs63750496(-;-)

From SNPedia
common in clinvar
Is agenotype
ofrs63750496
GeneMSH2
Chromosome2
Position47,429,809
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;-) 0 common in clinvar
(-;C) 6 Lynch syndrome, pathogenic mutation
(I;I) 0