ClinVar Miner

Submissions for variant NM_004070.4(CLCNKA):c.359-56C>T

gnomAD frequency: 0.01231  dbSNP: rs116036032
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001753125 SCV002007032 likely benign not provided 2020-06-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001753125 SCV005255826 likely benign not provided criteria provided, single submitter not provided

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