ClinVar Miner

Submissions for variant NM_021023.6(CFHR3):c.934A>T (p.Ile312Phe)

dbSNP: rs73073594
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000955826 SCV001102558 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002489328 SCV002799382 likely benign Hemolytic uremic syndrome, atypical, susceptibility to, 1; Age related macular degeneration 1 2022-04-06 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000955826 SCV005285427 benign not provided criteria provided, single submitter not provided

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