ClinVar Miner

Submissions for variant NM_001174150.2(ARL13B):c.1025-48G>A

gnomAD frequency: 0.00270  dbSNP: rs78946357
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 RCV000245847 SCV000316768 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001574957 SCV001801858 likely benign not provided 2019-03-01 criteria provided, single submitter clinical testing

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