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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ADAM17, IAH1
(D654N)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
ADAM17, IAH1
(V632I)
Single nucleotide variant
(missense variant)
Inflammatory skin and bowel disease, neonatal, 1
+1 more
GUncertain significance