List of variants reported as pathogenic for perceptual disorders by Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001029883.3(PCARE):c.1191G>A (p.Trp397Ter)	rs777103184	0.00001
NM_000260.4(MYO7A):c.496del (p.Glu166fs)	rs111033448
NM_000350.3(ABCA4):c.4838del (p.Asp1613fs)	rs61752438
NM_001034853.2(RPGR):c.2512del (p.Glu838fs)	rs2147197281
NM_004004.6(GJB2):c.231G>A (p.Trp77Ter)	rs80338944
NM_019098.5(CNGB3):c.1781+1G>T	rs1375507464
NM_206933.4(USH2A):c.5083del (p.Ser1695fs)	rs1553300016

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