Variants studied for EGFR-related lung cancer

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

If a variant has more than one submission, it may be counted in more than one significance column. If this is the case, the total number of variants will be less than the sum of the other cells.

pathogenic	likely pathogenic	uncertain significance	likely benign	benign	not provided	total
46	25	1378	1118	60	2	2626

Gene and significance breakdown #

Total genes and gene combinations: 2

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	not provided	total
EGFR	45	23	1319	1055	57	2	2498
EGFR, LOC126860048	1	2	59	63	3	0	128

Submitter and significance breakdown #

Total submitters: 3

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	not provided	total
Invitae	45	25	1378	1118	60	0	2626
GenomeConnect - Invitae Patient Insights Network	0	0	0	0	0	2	2
Thoracic Oncology Program, Dana-Farber Cancer Institute	1	0	0	0	0	0	1

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