ClinVar Miner

Submissions for variant NM_000186.4(CFH):c.791-20T>G

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002621587 SCV002950767 likely benign not provided 2024-10-24 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV005008660 SCV005629246 uncertain significance Basal laminar drusen; Factor H deficiency; Hemolytic uremic syndrome, atypical, susceptibility to, 1; Age related macular degeneration 4 2023-12-29 criteria provided, single submitter clinical testing

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