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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ONECUT2
(S164C)
Single nucleotide variant
(missense variant)
Autosomal dominant polycystic liver disease
GUncertain significance
ONECUT2
(P226A)
Single nucleotide variant
(missense variant)
Autosomal dominant polycystic liver disease
GUncertain significance
ONECUT2
(P310S)
Single nucleotide variant
(missense variant)
Autosomal dominant polycystic liver disease
GUncertain significance
ONECUT2
(R314W)
Single nucleotide variant
(missense variant)
Autosomal dominant polycystic kidney disease
GUncertain significance
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