List of variants in gene EGFR reported as likely pathogenic for brain glioma

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.1793G>C (p.Gly598Ala)	rs139236063
NM_005228.5(EGFR):c.1793G>T (p.Gly598Val)	rs139236063
NM_005228.5(EGFR):c.322A>G (p.Arg108Gly)	rs1057519888

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