ClinVar Miner

Submissions for variant NM_001256071.3(RNF213):c.715C>G (p.Gln239Glu)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV003421537 SCV004144530 likely benign not provided 2022-11-01 criteria provided, single submitter clinical testing RNF213: BP4
Labcorp Genetics (formerly Invitae), Labcorp RCV003421537 SCV004488402 benign not provided 2023-03-03 criteria provided, single submitter clinical testing

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