rs63750139(C;C)

common in clinvar

Is a	genotype
of	rs63750139
Gene	MSH6, FBXO11
Chromosome	2
Position	47,806,488
mentioned	by

Magnitude

0

Repute

Good

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