ClinVar Miner

Submissions for variant NM_001164688.2(RD3):c.-336AC[19]

dbSNP: rs34485370
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 RCV000401725 SCV000353922 uncertain significance Leber congenital amaurosis 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004691183 SCV005187205 uncertain significance not provided criteria provided, single submitter not provided

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