rs104894636(C;C)

common in clinvar

Is a	genotype
of	rs104894636
Gene	SGSH
Chromosome	17
Position	80,217,061
mentioned	by

Magnitude

0

Repute

Good

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