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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
UGT1A, UGT1A1
+8 more
(R108C)
Single nucleotide variant
(missense variant +1 more)
Hyperbilirubinemia
+4 more
GUncertain significance
UGT1A, UGT1A1
+8 more
(I370V +4 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
UGT1A, UGT1A1
+8 more
(M123I +4 more)
Single nucleotide variant
(missense variant)
Crigler-Najjar syndrome type 1
GUncertain significance
UGT1A, UGT1A1
+8 more
(R135L +4 more)
Single nucleotide variant
(missense variant)
Crigler-Najjar syndrome type 1
GUncertain significance
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