List of variants reported as uncertain significance for Autosomal dominant Alport syndrome by Neuberg Centre For Genomic Medicine, NCGM

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_000091.5(COL4A3):c.1459G>A (p.Gly487Ser)	rs745472969	0.00006
NM_000091.5(COL4A3):c.1127C>T (p.Pro376Leu)	rs760049264	0.00003
NM_000091.5(COL4A3):c.3949G>A (p.Val1317Met)	rs200017859	0.00003
NM_000091.5(COL4A3):c.1667C>T (p.Pro556Leu)	rs768989338	0.00002
NM_000091.5(COL4A3):c.3391G>A (p.Gly1131Ser)
NM_000091.5(COL4A3):c.398G>T (p.Gly133Val)	rs750189238
NM_000091.5(COL4A3):c.592G>A (p.Gly198Ser)

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