ClinVar Miner

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

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 3
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HGVS dbSNP
NM_000495.5(COL4A5):c.1033-6A>G rs869025330
NM_000495.5(COL4A5):c.4896T>G (p.Cys1632Trp) rs1569509336
NM_000495.5(COL4A5):c.81+4A>C rs1569469484

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