ClinVar Miner

Submissions for variant NM_020975.6(RET):c.1063+47G>A

gnomAD frequency: 0.00315  dbSNP: rs372177579
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 RCV001608244 SCV001834088 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV002465894 SCV002760464 likely benign not specified 2023-08-15 criteria provided, single submitter clinical testing

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