rs575830428

This variant is located in the EXT1 gene.

ClinVar annotation

Uncertain Significance☆☆☆
1 submitter1 publication

Multiple congenital exostosis

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About EXT1

This gene encodes an endoplasmic reticulum-resident type II transmembrane glycosyltransferase involved in the chain elongation step of heparan sulfate biosynthesis. Mutations in this gene cause the type I form of multiple exostoses. [provided by RefSeq, Jul 2008]

View all EXT1 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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