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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CXCR2
(P102L)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CXCR2
(R153H)
Single nucleotide variant
(missense variant)
CXCR2-related disorder
+1 more
GConflicting classifications of pathogenicity
CXCR2
(D293N)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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