ClinVar Miner

Submissions for variant NM_000168.6(GLI3):c.1648-220del

dbSNP: rs60699625
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 RCV001597830 SCV001831352 benign not provided 2019-08-18 criteria provided, single submitter clinical testing

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