rs104894639(G;G)

common in clinvar

Is a	genotype
of	rs104894639
Gene	SGSH
Chromosome	17
Position	80,210,622
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(A;G)	3	Carrier of a Sanfilippo syndrome type A mutation
(G;G)	0	common in clinvar