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rs63750712(CT;CT)

From SNPedia
common in clinvar
Is agenotype
ofrs63750712
GeneMSH2
Chromosome2
Position47,408,412
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;CT) 6 Lynch syndrome, pathogenic mutation
(CT;CT) 0 common in clinvar
(TC;TC) 0 common in clinvar