rs587779182(GT;GT)

common in clinvar

Is a	genotype
of	rs587779182
Gene	MSH2
Chromosome	2
Position	47,403,114
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(-;TG)	6	Likely miscall in 23andMe v5 data; otherwise, Lynch syndrome, pathogenic mutation
(GT;GT)	0	common in clinvar
(TG;TG)	0	common/normal