ClinVar Miner

Submissions for variant NM_000440.3(PDE6A):c.*241dup

dbSNP: rs36043437
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
Illumina Laboratory Services, Illumina RCV000349810 SCV000454666 likely benign Retinitis Pigmentosa, Recessive 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001672656 SCV001882682 benign not provided 2021-06-15 criteria provided, single submitter clinical testing

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