Variant: rs74315435

present in Gene: VSX1 present in Chromosome: 20 Position on Chromosome: 25077727 Alleles of this Variant: C/A

rs74315435 in VSX1 gene and CRANIOFACIAL ANOMALIES AND ANTERIOR SEGMENT DYSGENESIS SYNDROME PMID 15051220 2004 VSX1 (RINX) mutation with craniofacial anomalies, empty sella, corneal endothelial changes, and abnormal retinal and auditory bipolar cells.