ClinVar Miner

Submissions for variant NM_001256071.3(RNF213):c.10450G>A (p.Gly3484Ser)

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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 RCV003697320 SCV004467531 likely benign not provided 2023-07-26 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV003697320 SCV005408557 uncertain significance not provided 2023-12-06 criteria provided, single submitter clinical testing BP4_strong, PP2

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