ClinVar Miner

Submissions for variant NM_178857.6(RP1L1):c.564C>A (p.Leu188=)

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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 RCV003080675 SCV003486356 likely benign not provided 2024-11-11 criteria provided, single submitter clinical testing

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