ClinVar Miner

Submissions for variant NM_005228.5(EGFR):c.2626-12C>T

gnomAD frequency: 0.00001  dbSNP: rs775878427
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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 RCV002176382 SCV002471565 likely benign EGFR-related lung cancer 2024-07-15 criteria provided, single submitter clinical testing

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