rs63749831(AAT;AAT)

common in clinvar

Is a	genotype
of	rs63749831
Gene	MSH2
Chromosome	2
Position	47,475,051
mentioned	by

Magnitude

0

Repute

Good

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