rs745452577(G;G)

common in clinvar

Is a	genotype
of	rs745452577
Gene	HSPG2
Chromosome	1
Position	21,865,798
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(A;G)	1	Of uncertain significance relative to Schwartz Jampel syndrome according to ClinVar
(G;G)	0	common in clinvar