ClinVar Miner

Submissions for variant NM_001378414.1(HDAC4):c.1458C>T (p.Val486=)

gnomAD frequency: 0.00003  dbSNP: rs139841625
Minimum review status: Collection method:
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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) RCV000727899 SCV000855405 uncertain significance not provided 2017-07-13 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000727899 SCV001040274 likely benign not provided 2018-07-20 criteria provided, single submitter clinical testing

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