<b>Results</b>: We identified 15 distinct variants across 14 genes associated with non-syndromic retinitis pigmentosa, comprising 6 missense, 7 nonsense, 1 frameshift, and 2 splice-site variants, including 4 novel variants, i.e., p.(Val220Met) and p.(Pro1282SerfsTer2) in <i>RP1</i>, 1 each in <i>PDE6B</i> (c.2021+5G>A), and <i>PRCD</i> p.(Ser38Ter). The gene discussed is PDE6B; the disease is retinitis pigmentosa.