ClinVar Miner

Submissions for variant NM_003172.4(SURF1):c.321C>A (p.Ala107=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003511398 SCV004354741 likely benign Leigh syndrome 2024-11-05 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV005240816 SCV005885375 uncertain significance not specified 2025-02-28 criteria provided, single submitter clinical testing

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