ClinVar Miner

Submissions for variant NM_001378414.1(HDAC4):c.1979-209A>G

gnomAD frequency: 0.00712  dbSNP: rs146948927
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
GeneDx RCV001553062 SCV001773863 likely benign not provided 2018-12-24 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001553062 SCV005261885 likely benign not provided criteria provided, single submitter not provided

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