ClinVar Miner

Submissions for variant NM_005228.5(EGFR):c.2283+1G>A

dbSNP: rs397517104
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000038402 SCV000062074 uncertain significance not specified 2013-03-11 criteria provided, single submitter clinical testing

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