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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC10A1
(L35del)
Microsatellite
(inframe_deletion)
Hypercholanemia, familial, 2
+1 more
GUncertain significance
SLC10A1
(D24A)
Single nucleotide variant
(missense variant)
Hypercholanemia, familial, 2
GUncertain significance