ClinVar Miner

Submissions for variant NM_014444.5(TUBGCP4):c.1731+60G>C

dbSNP: rs2444036
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 RCV001620407 SCV001845836 benign not provided 2018-07-08 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001620407 SCV005290501 benign not provided criteria provided, single submitter not provided

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