ClinVar Miner

Submissions for variant NM_000283.4(PDE6B):c.993-49G>C

dbSNP: rs115328178
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 RCV001540961 SCV001758901 likely benign not provided 2019-01-13 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001540961 SCV005263601 likely benign not provided criteria provided, single submitter not provided

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