ClinVar Miner

Submissions for variant NM_005228.5(EGFR):c.1836C>T (p.Asp612=)

gnomAD frequency: 0.00001  dbSNP: rs150803480
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001505174 SCV001710066 likely benign EGFR-related lung cancer 2024-08-08 criteria provided, single submitter clinical testing

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