ClinVar Miner

Submissions for variant NM_001111.5(ADAR):c.*2323_*2330dup

dbSNP: rs113414804
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 RCV000405023 SCV000348488 uncertain significance Symmetrical dyschromatosis of extremities 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004691138 SCV005186924 uncertain significance not provided criteria provided, single submitter not provided

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