ClinVar Miner

List of variants reported as uncertain significance for Alport syndrome 1, X-linked recessive by Mendelics

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Total variants: 3

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HGVS	dbSNP
NM_000092.4(COL4A4):c.4760C>G (p.Pro1587Arg)	rs190148408
NM_033380.3(COL4A5):c.2858G>T (p.Gly953Val)	rs78972735
NM_033380.3(COL4A5):c.4599C>T (p.Cys1533=)	rs1603326524

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