ClinVar Miner

Submissions for variant NM_005228.5(EGFR):c.1818G>A (p.Leu606=)

gnomAD frequency: 0.00001  dbSNP: rs148242307
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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 RCV001502672 SCV001707506 likely benign EGFR-related lung cancer 2020-09-30 criteria provided, single submitter clinical testing

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