ClinVar Miner

List of variants reported as uncertain significance for Alport syndrome 1, X-linked recessive by Institute of Human Genetics, University of Leipzig Medical Center

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Total variants: 3

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HGVS	dbSNP
NM_033380.3(COL4A5):c.2215C>G (p.Pro739Ala)	rs104886164
NM_033380.3(COL4A5):c.3493G>A (p.Glu1165Lys)
NM_033380.3(COL4A5):c.4930T>C (p.Cys1644Arg)

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