ClinVar Miner

Submissions for variant NM_002150.3(HPD):c.1176C>T (p.Gly392=)

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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 RCV003788689 SCV004571169 likely benign Hawkinsinuria; Tyrosinemia type III 2023-09-15 criteria provided, single submitter clinical testing

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