ClinVar Miner

Submissions for variant NM_005228.5(EGFR):c.889+18G>T

gnomAD frequency: 0.00126  dbSNP: rs41323746
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute for Clinical Genetics, University Hospital TU Dresden, University Hospital TU Dresden RCV003238136 SCV002009718 uncertain significance not provided 2021-11-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002074057 SCV002415826 benign EGFR-related lung cancer 2024-02-01 criteria provided, single submitter clinical testing

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