ClinVar Miner

Submissions for variant NM_020975.6(RET):c.73+9385_73+9395del

dbSNP: rs368137511
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001550439 SCV001770766 likely benign not provided 2019-10-31 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 19666486)
Labcorp Genetics (formerly Invitae), Labcorp RCV002072038 SCV002384978 benign Multiple endocrine neoplasia, type 2 2022-11-22 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV004536174 SCV004749763 likely benign RET-related disorder 2020-06-15 no assertion criteria provided clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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