ClinVar Miner

Submissions for variant NM_001376.5(DYNC1H1):c.13007-178G>A

gnomAD frequency: 0.05728  dbSNP: rs868621403
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 RCV001616493 SCV001840228 benign not provided 2019-08-20 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001616493 SCV005294127 benign not provided criteria provided, single submitter not provided

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