ClinVar Miner

Submissions for variant NM_006204.4(PDE6C):c.-21C>T (rs374900090)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000363443 SCV000366055 uncertain significance Achromatopsia 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000392180 SCV000366056 uncertain significance Cone-Rod Dystrophy, Recessive 2016-06-14 criteria provided, single submitter clinical testing
Seelig Lab,University of Washington RCV000767309 SCV000897874 not provided not provided no assertion provided in vitro

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