ClinVar Miner

Submissions for variant NM_020975.6(RET):c.2731-13A>G

dbSNP: rs1223648532
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002088703 SCV002387565 likely benign Multiple endocrine neoplasia, type 2 2024-01-04 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV002088703 SCV004837535 likely benign Multiple endocrine neoplasia, type 2 2023-10-06 criteria provided, single submitter clinical testing

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