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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC10A2
(F304L)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
SLC10A2
(T130I)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
SLC10A2
(G77E)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
SLC10A2
(L44F)
Single nucleotide variant
(missense variant)
Bile acid malabsorption, primary, 1
+1 more
GConflicting classifications of pathogenicity
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