ClinVar Miner

Submissions for variant NM_005228.5(EGFR):c.2898C>T (p.Ile966=)

gnomAD frequency: 0.00002  dbSNP: rs142305759
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001501125 SCV001705930 likely benign EGFR-related lung cancer 2025-01-08 criteria provided, single submitter clinical testing

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