ClinVar Miner

Submissions for variant NM_001004356.3(FGFRL1):c.960C>A (p.Leu320=)

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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 RCV003012593 SCV003309004 likely benign not provided 2022-11-15 criteria provided, single submitter clinical testing

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