ClinVar Miner

Submissions for variant NM_177438.3(DICER1):c.5364+20A>T

gnomAD frequency: 0.00021  dbSNP: rs150893725
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV003738143 SCV004564898 benign not provided 2023-10-13 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV002268618 SCV002551472 likely benign not specified 2025-03-04 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002136727 SCV002410221 benign DICER1-related tumor predisposition 2025-02-04 criteria provided, single submitter clinical testing

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