ClinVar Miner

Submissions for variant NM_005228.5(EGFR):c.1208-17T>G

dbSNP: rs1785495534
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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 RCV002177232 SCV002349784 likely benign EGFR-related lung cancer 2022-09-27 criteria provided, single submitter clinical testing

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