List of variants reported as likely benign for Autosomal dominant Alport syndrome; Hematuria, benign familial, 2; Alport syndrome 3b, autosomal recessive by Fulgent Genetics, Fulgent Genetics

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000091.5(COL4A3):c.1483C>T (p.His495Tyr)	rs200510532	0.00110
NM_000091.5(COL4A3):c.2168C>T (p.Pro723Leu)	rs201198284	0.00021
NM_000091.5(COL4A3):c.63G>A (p.Leu21=)	rs1036829250	0.00008
NM_000091.5(COL4A3):c.1437C>T (p.Cys479=)	rs748691382	0.00003

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