List of variants reported as likely pathogenic for proteinuria by Centre for Mendelian Genomics, University Medical Centre Ljubljana

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000092.5(COL4A4):c.2320G>C (p.Gly774Arg)	rs569681869	0.00004
NM_000092.5(COL4A4):c.4394G>A (p.Gly1465Asp)	rs533297350	0.00003
NM_000085.5(CLCNKB):c.937_940dup (p.Arg314delinsLysTer)	rs779593707	0.00001
NM_022489.4(INF2):c.658G>A (p.Glu220Lys)	rs530391015
NM_033380.3(COL4A5):c.4906dup (p.Ile1636fs)	rs1556463583

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