ClinVar Miner

Submissions for variant NM_000283.4(PDE6B):c.1467+41C>T

gnomAD frequency: 0.02034  dbSNP: rs116283697
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 RCV001569276 SCV001793320 likely benign not provided 2018-11-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001569276 SCV005263604 likely benign not provided criteria provided, single submitter not provided

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