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rs267608078(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs267608078
GeneMSH6
Chromosome2
Position47,803,508
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;C) 6 Lynch syndrome, pathogenic mutation
(-;CC) 6 Lynch syndrome
(C;C) 0 common in clinvar