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rs63749831(AAT;AAT)

From SNPedia
common in clinvar
Is agenotype
ofrs63749831
GeneMSH2
Chromosome2
Position47,475,051
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;AAT) 6 Lynch syndrome, pathogenic mutation
(AAT;AAT) 0 common in clinvar