rs897471(C;C)

common in clinvar

Is a	genotype
of	rs897471
Gene	HSPG2
Chromosome	1
Position	21,864,961
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	0	Considered to be benign by ClinVar