ClinVar Miner

Submissions for variant NM_001148.6(ANK2):c.11033-38T>A

gnomAD frequency: 0.00036  dbSNP: rs141889990
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 RCV001533973 SCV001750856 likely benign not provided 2018-11-25 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001533973 SCV005256065 likely benign not provided criteria provided, single submitter not provided

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