rs587776705(GTG;GTG)

common in clinvar

Is a	genotype
of	rs587776705
Gene	MSH6
Chromosome	2
Position	47,803,633
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(-;GTG)	5	Variant of uncertain significance; possible Lynch syndrome mutation
(GTG;GTG)	0	common in clinvar