ClinVar Miner

List of variants reported as likely benign for Gilbert syndrome

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 7
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HGVS dbSNP gnomAD frequency
NM_000463.3(UGT1A1):c.*339G>C rs1042640 0.81209
NM_000463.3(UGT1A1):c.*211T>C rs10929303 0.73663
NM_000463.3(UGT1A1):c.*440G>C rs8330 0.72111
NM_001072.4(UGT1A6):c.862-9898G>A rs10929302 0.29868
UGT1A1*6 rs4148323 0.00891
NM_000463.3(UGT1A1):c.996+15T>C rs4148327 0.00099
NM_000463.3(UGT1A1):c.72G>A (p.Val24=) rs764918207 0.00002

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