ClinVar Miner

Submissions for variant NM_005228.5(EGFR):c.2284-18G>A

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV005158006 SCV005785253 likely benign EGFR-related lung cancer 2024-11-12 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV005249796 SCV005895739 likely benign Lung cancer 2024-10-16 criteria provided, single submitter clinical testing This variant is considered likely benign. This variant is intronic and is not expected to impact mRNA splicing.

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