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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EGFR
(L181F +3 more)
Single nucleotide variant
(missense variant)
EGFR-related lung cancer
GUncertain significance
EGFR
(P848L +3 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+4 more
GConflicting classifications of pathogenicity
EGFR
(G872R +3 more)
Single nucleotide variant
(missense variant)
EGFR-related lung cancer
GUncertain significance
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