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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CYP7A1, LOC110596866
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
CYP7A1, LOC110596866
(A13V)
Single nucleotide variant
(missense variant)
CYP7A1-related condition
+1 more
GConflicting classifications of pathogenicity
CYP7A1, LOC110596866
(G9R)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
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