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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)
not provided
GConflicting classifications of pathogenicity
CYP7A1, LOC110596866
(G9R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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