ClinVar Miner

Submissions for variant NM_001369.3(DNAH5):c.13126-39G>A

gnomAD frequency: 0.01324  dbSNP: rs78940762
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000250765 SCV000307702 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001589248 SCV001816965 likely benign not provided 2019-06-09 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001589248 SCV005259164 likely benign not provided criteria provided, single submitter not provided

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