ClinVar Miner

Submissions for variant NM_014053.4(FLVCR1):c.346C>T (p.Leu116=)

gnomAD frequency: 0.00003  dbSNP: rs150645228
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics RCV001288606 SCV001475859 uncertain significance not provided 2020-08-13 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001288606 SCV001605027 likely benign not provided 2023-10-13 criteria provided, single submitter clinical testing

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