rs63751426(C;C)

common in clinvar

Is a	genotype
of	rs63751426
Gene	MSH2
Chromosome	2
Position	47,410,205
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	6	Likely miscall in 23andMe v4 chip data; otherwise, Lynch syndrome, pathogenic mutation