List of variants in gene EGFR reported as not provided for Neoplasm of the large intestine

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.2170G>A (p.Gly724Ser)	rs1051753269	0.00001
NM_005228.5(EGFR):c.1476C>A (p.Ser492Arg)	rs1057519860
NM_005228.5(EGFR):c.2155G>A (p.Gly719Ser)	rs28929495

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