rs63751077(C;C)

common in clinvar

Is a	genotype
of	rs63751077
Gene	MSH6
Chromosome	2
Position	47,796,035
mentioned	by

Magnitude

0

Repute

Good

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