ClinVar Miner

Submissions for variant NM_177438.3(DICER1):c.5095+6G>A

gnomAD frequency: 0.00003  dbSNP: rs760384855
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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 RCV000229004 SCV000291705 likely benign DICER1-related tumor predisposition 2025-01-26 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002257602 SCV002533045 uncertain significance Hereditary cancer-predisposing syndrome 2022-03-09 criteria provided, single submitter curation

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