ClinVar Miner

List of variants reported as likely pathogenic for Alport syndrome 1, X-linked recessive by Research and Development, ARUP Laboratories

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Total variants: 3

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HGVS	dbSNP
NM_033380.3(COL4A5):c.1033-6A>G	rs869025330
NM_033380.3(COL4A5):c.4914T>G (p.Cys1638Trp)	rs1569509336
NM_033380.3(COL4A5):c.81+4A>C	rs1569469484

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