ClinVar Miner

Submissions for variant NM_004115.4(FGF14):c.*176dup

dbSNP: rs144061152
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 RCV000260102 SCV000382060 likely benign Autosomal dominant cerebellar ataxia 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001711917 SCV001940944 benign not provided 2021-05-12 criteria provided, single submitter clinical testing

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