ClinVar Miner

Submissions for variant NM_006915.3(RP2):c.903G>A (p.Glu301=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV005150484 SCV005773978 likely benign not provided 2024-03-02 criteria provided, single submitter clinical testing

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