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rs267608065(GT;GT)

From SNPedia
common in clinvar
Is agenotype
ofrs267608065
GeneMSH6
Chromosome2
Position47,800,331
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;GT) 6 Lynch syndrome, pathogenic mutation
(GT;GT) 0 common in clinvar
(TG;TG) 0 common in clinvar