ClinVar Miner

Submissions for variant NM_001352514.2(HLCS):c.1068G>C (p.Pro356=)

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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 RCV002590337 SCV002954430 likely benign Holocarboxylase synthetase deficiency 2022-10-19 criteria provided, single submitter clinical testing

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