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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
UGT1A, UGT1A1
+8 more
Microsatellite
(intron variant)
Crigler-Najjar syndrome, type II
+4 more
GConflicting classifications of pathogenicity; drug response; other
UGT1A3, UGT1A9
+8 more
(L15R)
Single nucleotide variant
(missense variant +1 more)
Crigler-Najjar syndrome, type II
+4 more
GLikely pathogenic
UGT1A, UGT1A1
+8 more
(G71R)
Single nucleotide variant
(intron variant +1 more)
Crigler-Najjar syndrome, type II
+4 more
GConflicting classifications of pathogenicity; drug response
UGT1A, UGT1A1
+8 more
Single nucleotide variant
(intron variant)
Bilirubin, serum level of, quantitative trait locus 1
+1 more
GBenign; association
UGT1A4, UGT1A5
+8 more
(Y486D +4 more)
Single nucleotide variant
(missense variant)
Crigler-Najjar syndrome, type II
+7 more
GPathogenic/Likely pathogenic
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