ClinVar Miner

Submissions for variant NM_005228.5(EGFR):c.2470-16G>T

gnomAD frequency: 0.00001  dbSNP: rs78746362
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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 RCV002023923 SCV002299556 likely benign EGFR-related lung cancer 2024-11-12 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV005247323 SCV005896765 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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