ClinVar Miner

Submissions for variant NM_005228.5(EGFR):c.2946+371G>A

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV003423587 SCV004162152 likely benign not provided 2025-01-01 criteria provided, single submitter clinical testing EGFR: BS2

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