List of variants in gene EGFR reported as uncertain significance for adenocarcinoma

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_005228.5(EGFR):c.2270A>G (p.Lys757Arg)	rs397517102	0.00002
NM_005228.5(EGFR):c.1661A>G (p.Glu554Gly)	rs779741928
NM_005228.5(EGFR):c.88+24313G>C

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