DisGeNET - a database of gene-disease associations

UGT1A9, UDP glucuronosyltransferase family 1 member A9, 54600

N. diseases: 94; N. variants: 310

Disease: Bilirubin level result ×

Variant: rs2602381 ×

Source: ALL

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _v

DPI _v

pLI

EI _vda

EL _gda

Score _vda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Variant

Gene

Disease

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs2602381

Entrez Id:	54575;54576;54600
Gene Symbol:	UGT1A10;UGT1A8;UGT1A9

UGT1A10;UGT1A8;UGT1A9

CUI:	C1287365
Disease:

Bilirubin level result

0.700

GeneticVariation

GWASDB

A genome-wide association study for serum bilirubin levels and gene-environment interaction in a Chinese population.

23371916

2013

dbSNP:

rs2602381

Entrez Id:	54575;54576;54600
Gene Symbol:	UGT1A10;UGT1A8;UGT1A9

UGT1A10;UGT1A8;UGT1A9

CUI:	C1287365
Disease:

Bilirubin level result

0.700

GeneticVariation

GWASDB

Genome-wide association meta-analysis for total serum bilirubin levels.

19414484

2009

dbSNP:

rs2602381

Entrez Id:	54575;54576;54600
Gene Symbol:	UGT1A10;UGT1A8;UGT1A9

UGT1A10;UGT1A8;UGT1A9

CUI:	C1287365
Disease:

Bilirubin level result

0.700

GeneticVariation

GWASDB

Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia.

19419973

2009