rs267607689(G;G)

common in clinvar

Is a	genotype
of	rs267607689
Gene	MSH2
Chromosome	2
Position	47,410,373
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(A;G)	6	Lynch syndrome, pathogenic mutation
(G;G)	0	common in clinvar
(G;T)	6	Lynch syndrome, pathogenic mutation