ClinVar Miner

Submissions for variant NM_005228.5(EGFR):c.1498+142C>T

gnomAD frequency: 0.72346  dbSNP: rs759162
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 RCV001685100 SCV001904665 benign not provided 2019-01-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001685100 SCV005268284 benign not provided criteria provided, single submitter not provided

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