rs367556910
This variant is located in the AMELX gene.
▶ClinVar annotation
About AMELX
This gene encodes a member of the amelogenin family of extracellular matrix proteins. Amelogenins are involved in biomineralization during tooth enamel development. Mutations in this gene cause X-linked amelogenesis imperfecta. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]
View all AMELX variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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