List of variants reported as uncertain significance for Alport syndrome by Molecular Genetics, Royal Melbourne Hospital

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000092.5(COL4A4):c.1668G>T (p.Lys556Asn)	rs764279454	0.00004
NM_000092.5(COL4A4):c.4394G>A (p.Gly1465Asp)	rs533297350	0.00004
NM_000091.5(COL4A3):c.3254T>G (p.Met1085Arg)	rs769395979	0.00001
NM_000092.5(COL4A4):c.2057-3T>G

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