ClinVar Miner

Submissions for variant NM_020975.6(RET):c.1264-7C>T

gnomAD frequency: 0.00002  dbSNP: rs772930754
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001487930 SCV001692429 likely benign Multiple endocrine neoplasia, type 2 2024-12-09 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV001487930 SCV004823491 likely benign Multiple endocrine neoplasia, type 2 2023-12-01 criteria provided, single submitter clinical testing

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