List of variants reported as likely pathogenic for perceptual disorders by Breakthrough Genomics, Breakthrough Genomics

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001319074.4(RAX2):c.411CCCGGG[3] (p.138PG[3])	rs549932754
NM_025114.4(CEP290):c.2274dup (p.Val759fs)
NM_025114.4(CEP290):c.5364+1G>A
NM_033629.6(TREX1):c.868_885del (p.Pro290_Ala295del)	rs79318303

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