ClinVar Miner

Submissions for variant NM_005228.5(EGFR):c.1580G>A (p.Arg527Gln)

gnomAD frequency: 0.00033  dbSNP: rs150477666
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001440803 SCV001643717 likely benign EGFR-related lung cancer 2024-01-27 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002257419 SCV002537320 likely benign Hereditary cancer-predisposing syndrome 2021-04-23 criteria provided, single submitter curation
ITMI RCV000120692 SCV000084853 not provided not specified 2013-09-19 no assertion provided reference population

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