ClinVar Miner

Submissions for variant NM_001370658.1(BTD):c.1311G>C (p.Val437=)

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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 RCV005197354 SCV005844149 likely benign Biotinidase deficiency 2024-12-24 criteria provided, single submitter clinical testing

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