ClinVar Miner

Submissions for variant NM_000168.6(GLI3):c.2104-50C>T

gnomAD frequency: 0.00406  dbSNP: rs115463742
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
PreventionGenetics, part of Exact Sciences RCV000249249 SCV000302801 likely benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001658159 SCV001874760 likely benign not provided 2021-01-22 criteria provided, single submitter clinical testing

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