ClinVar Miner

Submissions for variant NM_001206999.2(CIT):c.5543-49C>G

dbSNP: rs76850358
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
GeneDx RCV001598012 SCV001830329 benign not provided 2018-08-17 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001598012 SCV005233845 benign not provided criteria provided, single submitter not provided

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