ClinVar Miner

Submissions for variant NM_020975.6(RET):c.1522+20A>G

gnomAD frequency: 0.00001  dbSNP: rs1053383471
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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 RCV002105781 SCV002406238 likely benign Multiple endocrine neoplasia, type 2 2025-01-22 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV002268616 SCV002550384 likely benign not specified 2025-03-04 criteria provided, single submitter clinical testing

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