RS35003977 UGT1A1
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What This Variant Does
"CLNSIG=4
Associated Conditions
Hyperbilirubinemia
Crigler-Najjar syndrome
Gilbert syndrome
Lucey-Driscoll syndrome
Crigler-Najjar syndrome type 1
Inborn genetic diseases
UGT1A1-related disorder
type II
Hyperbilirubinemia
Crigler-Najjar syndrome
Gilbert syndrome
Lucey-Driscoll syndrome
Crigler-Najjar syndrome type 1
Inborn genetic diseases
UGT1A1-related disorder
Other Variants in UGT1A1