rs63751119(G;G)

common in clinvar

Is a	genotype
of	rs63751119
Gene	MSH2
Chromosome	2
Position	47,478,312
mentioned	by

Magnitude

0

Repute

Good

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