ClinVar Miner

Submissions for variant NM_005228.5(EGFR):c.1006+15G>A

gnomAD frequency: 0.00001  dbSNP: rs369345006
Minimum review status: Collection method:
Minimum conflict level:
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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 RCV002082725 SCV002326838 likely benign EGFR-related lung cancer 2025-01-29 criteria provided, single submitter clinical testing

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