List of variants reported as likely pathogenic for perceptual disorders by Genomic Research Center, Shahid Beheshti University of Medical Sciences

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Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_001038603.3(MARVELD2):c.1498C>T (p.Arg500Ter)	rs118203957	0.00009
NM_004086.3(COCH):c.1150C>T (p.Arg384Cys)	rs756541797	0.00006
NM_153676.4(USH1C):c.308G>A (p.Arg103His)	rs397514500	0.00006
NM_001146079.2(CLDN14):c.301G>A (p.Gly101Arg)	rs74315438	0.00004
NM_000260.4(MYO7A):c.439C>T (p.Arg147Cys)	rs782808261	0.00001
NM_000329.3(RPE65):c.556G>A (p.Asp186Asn)	rs1553153243
NM_001384140.1(PCDH15):c.4990dup (p.Met1664fs)	rs766484375
NM_014336.5(AIPL1):c.294del (p.Ile99fs)	rs1597331616
NM_016239.3(MYO15A):c.419dup (p.Phe141Valfs)	rs750130520
NM_080680.3(COL11A2):c.2754del (p.Gly919fs)	rs1562336726
NM_201253.3(CRB1):c.2389T>C (p.Ser797Pro)	rs1355198242

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