ClinVar Miner

Submissions for variant NM_020461.4(TUBGCP6):c.1983+158_1983+217del

dbSNP: rs1569115638
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001648759 SCV001861882 benign not provided 2019-01-13 criteria provided, single submitter clinical testing

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