rs63750675(G;G)

common in clinvar

Is a	genotype
of	rs63750675
Gene	MSH2
Chromosome	2
Position	47,466,774
mentioned	by

Magnitude

0

Repute

Good

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