List of variants in gene EGFR reported as uncertain significance for Lung cancer

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_005228.5(EGFR):c.3629C>T (p.Ala1210Val)	rs35918369	0.00034
NM_005228.5(EGFR):c.1936A>C (p.Ile646Leu)	rs140516819	0.00021
NM_005228.5(EGFR):c.3271+49del	rs17337514	0.00017
NM_005228.5(EGFR):c.1532C>A (p.Ser511Tyr)	rs371114444	0.00007
NM_005228.5(EGFR):c.3092G>A (p.Arg1031Gln)	rs570295933	0.00005
NM_005228.5(EGFR):c.2612C>A (p.Ala871Glu)	rs397517134
NM_005228.5(EGFR):c.2639G>C (p.Trp880Ser)	rs2534824129
NM_005228.5(EGFR):c.2701+1G>A	rs1787460755
NM_005228.5(EGFR):c.3272A>C (p.Glu1091Ala)	rs1788061731

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