ClinVar Miner

Submissions for variant NM_004698.4(PRPF3):c.1299A>G (p.Pro433=)

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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 RCV005069986 SCV005700803 likely benign not provided 2024-08-15 criteria provided, single submitter clinical testing

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