ClinVar Miner

Submissions for variant NM_005228.5(EGFR):c.425-4G>A

gnomAD frequency: 0.00004  dbSNP: rs181831531
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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 RCV000896008 SCV001040079 likely benign EGFR-related lung cancer 2024-01-10 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002258029 SCV002537705 likely benign Hereditary cancer-predisposing syndrome 2021-04-07 criteria provided, single submitter curation

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