ClinVar Miner

Submissions for variant NM_024753.5(TTC21B):c.*1123dup

dbSNP: rs886055020
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 RCV000341840 SCV000417557 uncertain significance Jeune thoracic dystrophy 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000393925 SCV000417558 uncertain significance Familial aplasia of the vermis 2016-06-14 criteria provided, single submitter clinical testing

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