rs886041667(-;-)

Schwartz Jampel syndrome type 1

Is a	genotype
of	rs886041667
Gene	HSPG2
Chromosome	1
Position	21,880,518
mentioned	by

Magnitude

7.8

Repute

Bad

Geno	Mag	Summary
(-;-)	7.8	Schwartz Jampel syndrome type 1
(CG;CG)	0	common in clinvar

See discussion and links via main rs-page