ClinVar Miner

Submissions for variant NM_001378414.1(HDAC4):c.339+10G>A

gnomAD frequency: 0.00002  dbSNP: rs199918439
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) RCV000335337 SCV000343738 uncertain significance not provided 2016-07-27 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000335337 SCV001020224 likely benign not provided 2024-12-07 criteria provided, single submitter clinical testing

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