ClinVar Miner

Submissions for variant NM_020975.6(RET):c.1064-6C>T

gnomAD frequency: 0.00004  dbSNP: rs768878280
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001079999 SCV000260322 likely benign Multiple endocrine neoplasia, type 2 2024-12-12 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV000679708 SCV000806993 likely benign not provided 2017-11-07 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV001079999 SCV004357226 likely benign Multiple endocrine neoplasia, type 2 2023-02-15 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV001079999 SCV004822632 likely benign Multiple endocrine neoplasia, type 2 2024-02-05 criteria provided, single submitter clinical testing

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