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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC10A2
(P251L)
Single nucleotide variant
(missense variant)
Bile acid malabsorption, primary, 1
+1 more
GUncertain significance
SLC10A2
(C106*)
Single nucleotide variant
(nonsense)
Bile acid malabsorption, primary, 1
+1 more
GConflicting classifications of pathogenicity