ClinVar Miner

Submissions for variant NM_020975.6(RET):c.2731-8C>G

dbSNP: rs1564499958
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000679737 SCV000807037 likely benign not provided 2017-03-21 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001443766 SCV001646751 likely benign Multiple endocrine neoplasia, type 2 2023-06-27 criteria provided, single submitter clinical testing

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