ClinVar Miner

Submissions for variant NM_153638.4(PANK2):c.264C>T (p.Gly88=)

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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 RCV003612738 SCV004486758 likely benign Pigmentary pallidal degeneration 2024-02-17 criteria provided, single submitter clinical testing

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