ClinVar Miner

Submissions for variant NM_020975.6(RET):c.73+53G>A

gnomAD frequency: 0.37468  dbSNP: rs12267460
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001609513 SCV001841614 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Genetics and Molecular Pathology, SA Pathology RCV002466688 SCV002761350 benign Multiple endocrine neoplasia type 2A 2019-08-06 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001609513 SCV005317088 benign not provided criteria provided, single submitter not provided

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