rs63750408(T;T)

common in clinvar

Is a	genotype
of	rs63750408
Gene	MSH2
Chromosome	2
Position	47,410,135
Merged from	Rs776948651
mentioned	by

Magnitude

0

Repute

Good

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