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rs267608094(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs267608094
GeneFBXO11, MSH6
Chromosome2
Position47,806,641
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 6 Lynch syndrome, pathogenic mutation