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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ABCB11
(E297G)
Single nucleotide variant
(missense variant)
Progressive familial intrahepatic cholestasis type 2
+4 more
GPathogenic
ABCB11
(A151T)
Single nucleotide variant
(missense variant)
Benign recurrent intrahepatic cholestasis type 2
+1 more
GUncertain significance