ClinVar Miner

Submissions for variant NM_001378414.1(HDAC4):c.339+8G>A

gnomAD frequency: 0.08617  dbSNP: rs2290092
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001609503 SCV001841603 benign not provided 2018-12-22 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001609503 SCV002476248 benign not provided 2025-02-02 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001609503 SCV005239752 benign not provided criteria provided, single submitter not provided

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