rs2507570565
This variant is located in the ZNF469 gene.
▶ClinVar annotation
Likely Benign★☆☆☆
1 submitter1 publicationAbout ZNF469
This gene encodes a zinc-finger protein. Low-percent homology to certain collagens suggests that it may function as a transcription factor or extra-nuclear regulator factor for the synthesis or organization of collagen fibers. Mutations in this gene cause brittle cornea syndrome. [provided by RefSeq, Jul 2008]
View all ZNF469 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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