rs137853248(G;G)

common in clinvar

Is a	genotype
of	rs137853248
Gene	HSPG2
Chromosome	1
Position	21,864,874
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(A;A)	7.8	Schwartz Jampel syndrome type 1
(A;G)	3	Carrier for a Schwartz Jampel syndrome mutation
(G;G)	0	common in clinvar