ClinVar Miner

Submissions for variant NM_022081.6(HPS4):c.1341T>G (p.Pro447=)

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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 RCV003678695 SCV004427366 likely benign not provided 2023-01-19 criteria provided, single submitter clinical testing

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