List of variants reported as likely pathogenic for hematuria, benign familial, 1 by Juno Genomics, Hangzhou Juno Genomics, Inc

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_000092.5(COL4A4):c.2752G>A (p.Gly918Arg)	rs372606845	0.00002
NM_000092.5(COL4A4):c.1921C>T (p.Arg641Ter)	rs778345125	0.00001
NM_000092.5(COL4A4):c.134del (p.Gly45fs)
NM_000092.5(COL4A4):c.1938_1941dup (p.Gly648fs)
NM_000092.5(COL4A4):c.2447G>A (p.Gly816Glu)
NM_000092.5(COL4A4):c.3206G>A (p.Gly1069Glu)	rs2150172344
NM_000092.5(COL4A4):c.595G>A (p.Gly199Arg)

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