ClinVar Miner

Submissions for variant NM_005228.5(EGFR):c.-216G>T

dbSNP: rs712829
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001656223 SCV001862376 benign not provided 2019-01-10 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 24137392, 16885506, 20621735, 15665278, 21292812)
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV003316845 SCV004017413 likely benign Lung cancer 2023-07-07 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001656223 SCV005267633 benign not provided criteria provided, single submitter not provided

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