ClinVar Miner

Submissions for variant NM_001386393.1(PANK2):c.30G>A (p.Leu10=)

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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 RCV003503143 SCV004322566 likely benign Pigmentary pallidal degeneration 2023-11-21 criteria provided, single submitter clinical testing

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