rs63750245(C;C)

common in clinvar

Is a	genotype
of	rs63750245
Gene	MSH2
Chromosome	2
Position	47,416,383
Merged from	Rs193922371
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	6	Lynch syndrome, pathogenic mutation
(T;T)	7	Lynch syndrome; hereditary nonpolyposis colorectal cancer-1