ClinVar Miner

Submissions for variant NM_001378414.1(HDAC4):c.2346C>T (p.Cys782=)

gnomAD frequency: 0.00010  dbSNP: rs144099208
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000278273 SCV000342157 uncertain significance not provided 2016-06-30 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000278273 SCV003007109 likely benign not provided 2024-03-19 criteria provided, single submitter clinical testing

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