ClinVar Miner

Submissions for variant NM_003172.4(SURF1):c.55-5C>T

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV002510346 SCV002819517 uncertain significance not specified 2022-12-13 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002571597 SCV003022639 likely benign Leigh syndrome 2022-12-16 criteria provided, single submitter clinical testing

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