ClinVar Miner

Submissions for variant NM_005228.5(EGFR):c.2946+20C>T

gnomAD frequency: 0.00003  dbSNP: rs746554400
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002146504 SCV002465929 likely benign EGFR-related lung cancer 2024-12-21 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004706412 SCV005227384 likely benign not provided criteria provided, single submitter not provided

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