ClinVar Miner

Submissions for variant NM_003172.4(SURF1):c.798T>C (p.Thr266=)

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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 RCV002594630 SCV002949509 likely benign Leigh syndrome 2022-10-13 criteria provided, single submitter clinical testing

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