List of variants reported as uncertain significance for X-linked Alport syndrome by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_033380.3(COL4A5):c.4162G>A (p.Gly1388Ser)	rs2524616692	0.00001
NM_033380.3(COL4A5):c.4693C>G (p.Pro1565Ala)	rs104886295	0.00001
NM_033380.3(COL4A5):c.1883C>T (p.Pro628Leu)	rs281874682
NM_033380.3(COL4A5):c.2308G>C (p.Ala770Pro)	rs2066736056
NM_033380.3(COL4A5):c.2365A>T (p.Thr789Ser)	rs963596952
NM_033380.3(COL4A5):c.3853G>A (p.Gly1285Ser)	rs764755602

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