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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TGFB1
(R218H)
Single nucleotide variant
(missense variant)
not provided
+2 more
GPathogenic
TGFB1
(D191fs)
Deletion
(frameshift variant)
Inflammatory bowel disease, immunodeficiency, and encephalopathy
GLikely pathogenic