ClinVar Miner

Submissions for variant NM_000311.5(PRNP):c.162T>C (p.Gly54=)

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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 RCV005165031 SCV005796956 likely benign Huntington disease-like 1 2024-04-01 criteria provided, single submitter clinical testing

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