List of variants reported as pathogenic for CNGA3-related retinopathy by Al Jalila Children’s Genomics Center, Al Jalila Childrens Speciality Hospital

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001298.3(CNGA3):c.967G>C (p.Ala323Pro)	rs146195955	0.00033
NM_001298.3(CNGA3):c.1495C>T (p.Arg499Ter)	rs1386641968	0.00002
NM_001298.3(CNGA3):c.847C>T (p.Arg283Trp)	rs104893613	0.00002
NM_001298.3(CNGA3):c.1114C>T (p.Pro372Ser)	rs1464167194	0.00001

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