ClinVar Miner

Submissions for variant NM_001004356.3(FGFRL1):c.477G>C (p.Val159=)

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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 RCV005189301 SCV005848006 likely benign not provided 2024-09-05 criteria provided, single submitter clinical testing

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