ClinVar Miner

Submissions for variant NM_001034850.3(RETREG1):c.874-27C>T

dbSNP: rs73042393
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 RCV001677317 SCV001894252 benign not provided 2018-12-17 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001677317 SCV005299171 benign not provided criteria provided, single submitter not provided

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