ClinVar Miner

Submissions for variant NM_018026.4(PACS1):c.2811G>A (p.Lys937=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV004701108 SCV005204581 likely benign not specified 2024-06-19 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV005103583 SCV005818883 likely benign Schuurs-Hoeijmakers syndrome 2024-06-11 criteria provided, single submitter clinical testing

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