ClinVar Miner

Submissions for variant NM_001378414.1(HDAC4):c.2921T>C (p.Val974Ala)

gnomAD frequency: 0.00002  dbSNP: rs554154260
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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 RCV000894723 SCV001038725 likely benign not provided 2017-08-14 criteria provided, single submitter clinical testing

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