Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs267608050(T;T)

From SNPedia
(Redirected from I5037858(I;I))
common in clinvar
Is agenotype
ofrs267608050
GeneMSH6
Chromosome2
Position47,799,767
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;T) 6 Lynch syndrome, pathogenic mutation
(T;T) 0 common in clinvar