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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
IFNAR2, IFNAR2-IL10RB
(D439N)
Single nucleotide variant
(3 prime UTR variant +1 more)
not provided
GUncertain significance
IFNAR2-IL10RB, IL10RB
(V148M)
Single nucleotide variant
(missense variant)
Inflammatory bowel disease 25
+2 more
GConflicting classifications of pathogenicity