ClinVar Miner

List of variants reported as likely benign 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: 4
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HGVS dbSNP
NM_000495.5(COL4A5):c.1855C>T (p.Pro619Ser) rs1569494314
NM_000495.5(COL4A5):c.2858G>T (p.Gly953Val) rs78972735
NM_000495.5(COL4A5):c.4282C>A (p.Leu1428Met) rs1569508163
NM_000495.5(COL4A5):c.891+9T>G

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