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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
IL19, LOC128462409
+1 more
(H32N)
Single nucleotide variant
(missense variant +2 more)
not provided
+1 more
GUncertain significance
IL10, IL19
+1 more
(G15R)
Single nucleotide variant
(missense variant +2 more)
Inflammatory bowel disease
+4 more
GConflicting classifications of pathogenicity