NM_001034853.2(RPGR):c.485_486del (p.Phe162TyrfsTer4) is a frameshift variant due to a 2-nucleotide deletion resulting in a premature stop codon after 4 amino acids within exon 6 of 15, which is predicted to trigger nonsense-mediated decay (PVS1). This variant is absent from gnomAD v4.1.0 (PM2_Supporting). This variant has been reported in at least 2 apparently unrelated probands meeting one of the PS4 requirements of a male with some functional vision impairment by age 30 years and/or decreased or absent electroretinogram responses, or a female with functional visual abnormality and documentation of a male relative affected with retinitis pigmentosa (PMID: 17325176, PMID: 32795431; PS4_Supporting). At least one proband harboring this variant exhibits a phenotype including onset in the first or second decade of life (1 pt), night blindness (0.5 pts), reduced visual acuity (0.5 pts), visual field constriction (0.5 pts), and myopia (0.5 pts), with a family history consistent with X-linked inheritance (2 pts), which together are specific for RPGR-related retinopathy (5 points, PMID: 26197217, PP4). The variant has been reported to segregate with retinal dystrophy through at least 6 affected meioses from 1 family (PP1_Moderate; PMID: 26197217). In summary, this variant is classified as pathogenic for RPGR-related retinopathy based on the ClinGen X-linked Inherited Retinal Disease Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines for RPGR Version 1.0.0; PVS1, PS4_Supporting, PM2_Supporting, PP1_Moderate, and PP4.