ClinVar Miner

Submissions for variant NM_001164688.2(RD3):c.*1582del

dbSNP: rs879756831
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 RCV000311683 SCV000353883 uncertain significance Leber congenital amaurosis 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004691180 SCV005187198 uncertain significance not provided criteria provided, single submitter not provided

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