ClinVar Miner

Submissions for variant NM_020975.6(RET):c.1880-16C>T

gnomAD frequency: 0.00012  dbSNP: rs370491323
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002209035 SCV002352318 benign Multiple endocrine neoplasia, type 2 2025-01-26 criteria provided, single submitter clinical testing

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