ClinVar Miner

Submissions for variant NM_001378414.1(HDAC4):c.1294+10A>G

gnomAD frequency: 0.12308  dbSNP: rs10207474
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 RCV001661255 SCV001874567 benign not provided 2018-11-08 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001661255 SCV002442182 benign not provided 2025-01-22 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001661255 SCV005239737 benign not provided criteria provided, single submitter not provided

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