ClinVar Miner

Submissions for variant NM_001378414.1(HDAC4):c.1434C>T (p.Asn478=)

gnomAD frequency: 0.00005  dbSNP: rs754530774
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) RCV000174350 SCV000225636 uncertain significance not provided 2015-02-10 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000174350 SCV003459679 likely benign not provided 2022-09-07 criteria provided, single submitter clinical testing

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