ClinVar Miner

List of variants in gene combination UGT1A, UGT1A1, UGT1A10, UGT1A3, UGT1A4, UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9 reported as uncertain significance for abdominal and pelvic region disorder

Included ClinVar conditions (961):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 38
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HGVS dbSNP
NM_000463.3(UGT1A1):c.*133G>A
NM_000463.3(UGT1A1):c.*188T>G
NM_000463.3(UGT1A1):c.*269C>T
NM_000463.3(UGT1A1):c.*301G>A
NM_000463.3(UGT1A1):c.*419T>C
NM_000463.3(UGT1A1):c.*461G>T
NM_000463.3(UGT1A1):c.*674G>A
NM_000463.3(UGT1A1):c.*84T>C
NM_000463.3(UGT1A1):c.1180T>C (p.Phe394Leu)
NM_000463.3(UGT1A1):c.1410C>T (p.Gly470=)
NM_000463.3(UGT1A1):c.1411G>A (p.Ala471Thr)
NM_000463.3(UGT1A1):c.1518C>A (p.Thr506=)
NM_000463.3(UGT1A1):c.1548A>T (p.Lys516Asn)
NM_000463.3(UGT1A1):c.25C>T (p.Arg9Cys)
NM_000463.3(UGT1A1):c.288G>A (p.Gly96=)
NM_000463.3(UGT1A1):c.361G>C (p.Ala121Pro)
NM_000463.3(UGT1A1):c.584G>A (p.Arg195Lys)
NM_000463.3(UGT1A1):c.964A>G (p.Ile322Val)
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.862-5909T>G rs754213125
NM_001072.4(UGT1A6):c.862-5999T>C rs57307513
NM_001072.4(UGT1A6):c.862-6073T>G rs35003977
NM_001072.4(UGT1A6):c.862-6170G>A rs375974892
NM_001072.4(UGT1A6):c.862-6207A>G rs148755655
NM_001072.4(UGT1A6):c.862-6270C>T rs199766420
NM_001072.4(UGT1A6):c.862-6361A>G rs1191873899
NM_001072.4(UGT1A6):c.862-6421T>C rs144217005
NM_001072.4(UGT1A6):c.862-6447T>C rs374655757
NM_001072.4(UGT1A6):c.862-6453T>C rs138183896
NM_001072.4(UGT1A6):c.862-6558C>T rs191471887
NM_001072.4(UGT1A6):c.862-6580A>C rs140365717
NM_001072.4(UGT1A6):c.862-6605C>G rs747942373
NM_001072.4(UGT1A6):c.862-6606C>T rs34526305

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