List of variants reported as likely benign for perceptual disorders by Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_006269.2(RP1):c.1118C>T (p.Thr373Ile)	rs77775126	0.00985
NM_019098.5(CNGB3):c.1208G>A (p.Arg403Gln)	rs147876778	0.00119
NM_000329.3(RPE65):c.394G>A (p.Ala132Thr)	rs61752878	0.00103

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