rs989994(C;C)

common in complete genomics

Is a	genotype
of	rs989994
Gene	HSPG2
Chromosome	1
Position	21,880,156
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(C;C)	0	common in complete genomics
(C;T)	0	Considered benign in ClinVar
(T;T)	0	common in clinvar