List of variants reported as likely pathogenic for autosomal dominant Alport syndrome by Institute of Human Genetics, Cologne University

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_000091.5(COL4A3):c.1409G>A (p.Gly470Glu)	rs2125982395
NM_000091.5(COL4A3):c.205G>T (p.Glu69Ter)	rs1574658390
NM_000091.5(COL4A3):c.2981G>A (p.Gly994Asp)	rs1574803132
NM_000092.5(COL4A4):c.3101C>A (p.Ser1034Ter)	rs1576129421
NM_000092.5(COL4A4):c.595G>T (p.Gly199Ter)	rs750345987
NM_000092.5(COL4A4):c.903dup (p.Gly302fs)	rs1559628183

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