ClinVar Miner

Submissions for variant NM_005228.5(EGFR):c.3272-123G>A

gnomAD frequency: 0.83662  dbSNP: rs2692456
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001676139 SCV001895070 benign not provided 2019-01-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001676139 SCV005273258 benign not provided criteria provided, single submitter not provided

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