List of variants in gene EGFR reported as uncertain significance by Genetic Services Laboratory, University of Chicago

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_005228.5(EGFR):c.3467A>C (p.His1156Pro)	rs149174093	0.00062
NM_005228.5(EGFR):c.2543C>T (p.Pro848Leu)	rs148934350	0.00026
NM_005228.5(EGFR):c.493C>T (p.Arg165Trp)	rs587778252	0.00008
NM_005228.5(EGFR):c.1900G>A (p.Glu634Lys)	rs765068810	0.00004
NM_005228.5(EGFR):c.2492G>A (p.Arg831His)	rs150036236	0.00003
NM_005228.5(EGFR):c.1933T>C (p.Ser645Pro)	rs1584222146
NM_005228.5(EGFR):c.2575G>T (p.Ala859Ser)

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