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rs778653296(C;C)

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common in clinvar

Is a	genotype
of	rs778653296
Gene	HSPG2
Chromosome	1
Position	21,851,790
mentioned	by

0

Good

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

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Is a genotype