rs1230845124
This variant is located in the VSX2 gene.
▶ClinVar annotation
About VSX2
This gene encodes a homeobox protein originally described as a retina-specific transcription factor. Mutations in this gene are associated with microphthalmia, cataracts and iris abnormalities. [provided by RefSeq, Oct 2009]
View all VSX2 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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