ClinVar Miner

List of variants in gene combination UGT1A, UGT1A1, UGT1A10, UGT1A3, UGT1A4, UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9 reported as uncertain significance for Gilbert syndrome

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 10
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HGVS dbSNP
NM_001072.4(UGT1A6):c.*201G>A rs541532523
NM_001072.4(UGT1A6):c.*585G>T rs886055800
NM_001072.4(UGT1A6):c.1119T>C (p.Gly373=) rs139698110
NM_001072.4(UGT1A6):c.1204C>T (p.Arg402Cys) rs778766461
NM_001072.4(UGT1A6):c.1319T>C (p.Met440Thr) rs202172337
NM_001072.4(UGT1A6):c.1321C>T (p.Arg441Cys) rs143033456
NM_001072.4(UGT1A6):c.862-6073T>G rs35003977
NM_001072.4(UGT1A6):c.862-6270C>T rs199766420
NM_001072.4(UGT1A6):c.862-6447T>C rs374655757
NM_001072.4(UGT1A6):c.862-6453T>C rs138183896

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