List of variants reported as uncertain significance for X-linked Alport syndrome by Institute of Human Genetics, University of Leipzig Medical Center

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_033380.3(COL4A5):c.2215C>G (p.Pro739Ala)	rs104886164	0.00034
NM_033380.3(COL4A5):c.4246C>T (p.Arg1416Cys)	rs104886270	0.00008
NM_033380.3(COL4A5):c.3493G>A (p.Glu1165Lys)	rs771538814	0.00002
NM_033380.3(COL4A5):c.4895C>T (p.Ser1632Leu)	rs1556463567
NM_033380.3(COL4A5):c.4930T>C (p.Cys1644Arg)	rs866393484

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