List of variants in gene EGFR reported as benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_005228.5(EGFR):c.2361G>A (p.Gln787=)	rs1050171	0.51617
NM_005228.5(EGFR):c.1887T>A (p.Thr629=)	rs2227984	0.33239
NM_005228.5(EGFR):c.2709= (p.Thr903=)	rs1140475	0.10499
NM_005228.5(EGFR):c.1839C>T (p.Ala613=)	rs17290169	0.05521
NM_005228.5(EGFR):c.2508C>T (p.Arg836=)	rs2229066

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