ClinVar Miner

Submissions for variant NM_001206999.2(CIT):c.1665+40T>C

gnomAD frequency: 0.47825  dbSNP: rs440299
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 RCV001649296 SCV001862960 benign not provided 2018-07-06 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001649296 SCV005234325 benign not provided criteria provided, single submitter not provided

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