List of variants reported as uncertain significance for pigmented paravenous retinochoroidal atrophy by Centre for Mendelian Genomics, University Medical Centre Ljubljana

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_201253.3(CRB1):c.4006-10A>G	rs766850702	0.00001
NM_201253.3(CRB1):c.3878+9C>T	rs1571564812
NM_201253.3(CRB1):c.523G>A (p.Val175Ile)	rs1166808508
NM_201253.3(CRB1):c.527C>T (p.Pro176Leu)	rs1417370819

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