ClinVar Miner

Submissions for variant NM_005228.5(EGFR):c.2469+13G>A

dbSNP: rs764099332
Minimum review status: Collection method:
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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 RCV002217516 SCV002370619 likely benign EGFR-related lung cancer 2024-07-08 criteria provided, single submitter clinical testing

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