ClinVar Miner

Submissions for variant NM_147127.5(EVC2):c.1710+224C>A

dbSNP: rs112417127
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 RCV001587127 SCV001820790 likely benign not provided 2019-06-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001587127 SCV005256666 likely benign not provided criteria provided, single submitter not provided

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