ClinVar Miner

Submissions for variant NM_003172.4(SURF1):c.511C>T (p.Leu171=)

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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 RCV003620109 SCV004391135 likely benign Leigh syndrome 2022-11-28 criteria provided, single submitter clinical testing

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