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)

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
66	32	1619	1378	60	4	3155

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	64	30	1555	1299	57	4	3005
EGFR, LOC126860048	2	2	64	79	3	0	150

Submitter and significance breakdown #

Total submitters: 3

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	not provided	total
Labcorp Genetics (formerly Invitae), Labcorp	66	32	1619	1378	60	0	3155
GenomeConnect - Invitae Patient Insights Network	0	0	0	0	0	4	4
Thoracic Oncology Program, Dana-Farber Cancer Institute	1	0	0	0	0	0	1

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