rs63750161(AG;AG)

common in clinvar

Is a	genotype
of	rs63750161
Gene	MSH2
Chromosome	2
Position	47,463,091
mentioned	by

Magnitude

0

Repute

Good

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