DisGeNET - a database of gene-disease associations

Source: GWASCAT

Variants associated to the Disease: Bilirubin measurement ×

Variants associated to the Gene: UGT1A9 ×

Results per page

Gene

Disease

Variant

Source

DSI _v

DPI _v

pLI

Consequence

AF_EXOME

AF_GENOME

Variant	Gene	DSI _v	DPI _v	Chr	Position	Consequence	Alleles	Class	AF EXOME	AF GENOME	Num. diseases
rs4148325	UGT1A8 ; UGT1A5 ; UGT1A10 ; UGT1A7 ; UGT1A1 ; UGT1A9 ; UGT1A3 ; UGT1A4 ; UGT1A6	0.851	0.080	2	233764663	intron variant	C/T	snv		0.36	8
rs887829	UGT1A8 ; UGT1A5 ; UGT1A6 ; UGT1A7 ; UGT1A4 ; UGT1A3 ; UGT1A10 ; UGT1A1 ; UGT1A9	0.763	0.280	2	233759924	intron variant	C/T	snv		0.36	8
rs929596	UGT1A5 ; UGT1A4 ; UGT1A9 ; UGT1A10 ; UGT1A8 ; UGT1A7 ; UGT1A6 ; UGT1A3 ; UGT1A1	0.925	0.040	2	233765830	intron variant	A/G	snv		0.32	7
rs17863787	UGT1A9 ; UGT1A8 ; UGT1A6 ; UGT1A7 ; UGT1A10	0.925	0.040	2	233702448	intron variant	T/G	snv		0.30	7
rs4663969	UGT1A6 ; UGT1A9 ; UGT1A3 ; UGT1A10 ; UGT1A5 ; UGT1A4 ; UGT1A8 ; UGT1A7	1.000		2	233746667	intron variant	C/A;T	snv			5
rs3755319	UGT1A8 ; UGT1A1 ; UGT1A3 ; UGT1A4 ; UGT1A7 ; UGT1A10 ; UGT1A9 ; UGT1A5 ; UGT1A6	0.925	0.120	2	233758936	intron variant	A/C;G;T	snv			5
rs4477910	UGT1A9 ; UGT1A10 ; UGT1A7 ; UGT1A4 ; UGT1A8 ; UGT1A5 ; UGT1A6 ; UGT1A3	1.000		2	233735091	intron variant	A/T	snv		0.46	5
rs1875263	UGT1A9 ; UGT1A5 ; UGT1A10 ; UGT1A7 ; UGT1A6 ; UGT1A8 ; UGT1A4	1.000		2	233716976	intron variant	C/G;T	snv			5
rs10173355	UGT1A9 ; UGT1A7 ; UGT1A10 ; UGT1A8	1.000		2	233688675	intron variant	A/G;T	snv			5
rs2070959	UGT1A8 ; UGT1A7 ; UGT1A9 ; UGT1A10 ; UGT1A6	0.742	0.320	2	233693545	missense variant	A/G	snv	0.31	0.30	3
rs11695484	DNAJB3 ; UGT1A3 ; UGT1A8 ; UGT1A7 ; UGT1A9 ; UGT1A6 ; UGT1A10 ; UGT1A4 ; UGT1A5			2	233745803	intron variant	A/G	snv		0.30	2
rs4148324	UGT1A10 ; UGT1A3 ; UGT1A6 ; UGT1A4 ; UGT1A7 ; UGT1A8 ; UGT1A9 ; UGT1A5 ; UGT1A1			2	233764076	intron variant	T/A;G	snv		0.36	2
rs6747843	UGT1A10 ; UGT1A8 ; UGT1A6 ; UGT1A5 ; UGT1A4 ; LOC100286922 ; UGT1A9 ; UGT1A7 ; UGT1A3			2	233755708	non coding transcript exon variant	G/A	snv		0.30	2
rs6742078	UGT1A3 ; UGT1A7 ; UGT1A8 ; UGT1A10 ; UGT1A6 ; UGT1A4 ; UGT1A9 ; UGT1A1 ; UGT1A5	0.807	0.240	2	233763993	intron variant	G/T	snv		0.36	2
rs6714634	UGT1A3 ; UGT1A8 ; UGT1A10 ; UGT1A6 ; UGT1A7 ; LOC100286922 ; UGT1A5 ; UGT1A9 ; UGT1A4			2	233756119	non coding transcript exon variant	T/C	snv		0.30	2
rs3771341	UGT1A4 ; UGT1A10 ; UGT1A6 ; UGT1A3 ; UGT1A5 ; UGT1A8 ; UGT1A9 ; UGT1A7 ; UGT1A1			2	233764593	intron variant	G/A;T	snv		0.33	2
rs10179091	UGT1A4 ; UGT1A3 ; UGT1A5 ; UGT1A6 ; UGT1A7 ; UGT1A8 ; UGT1A10 ; UGT1A9			2	233749337	intron variant	T/C	snv		0.49	2
rs17864701	UGT1A4 ; UGT1A3 ; UGT1A6 ; UGT1A8 ; UGT1A7 ; UGT1A5 ; DNAJB3 ; UGT1A9 ; UGT1A10			2	233744071	intron variant	C/T	snv		0.30	2
rs10178992	UGT1A5 ; UGT1A3 ; UGT1A10 ; UGT1A8 ; UGT1A4 ; UGT1A9 ; UGT1A7 ; UGT1A6			2	233749231	intron variant	T/A	snv		0.37	2
rs6431630	UGT1A5 ; UGT1A4 ; UGT1A6 ; UGT1A8 ; UGT1A1 ; UGT1A10 ; UGT1A7 ; UGT1A3 ; UGT1A9			2	233768740	intron variant	G/A	snv		0.18	2
rs17862875	UGT1A6 ; UGT1A10 ; UGT1A5 ; UGT1A8 ; UGT1A3 ; UGT1A9 ; UGT1A4 ; UGT1A7			2	233740656	intron variant	G/A	snv		0.30	2
rs10929301	UGT1A6 ; UGT1A7 ; UGT1A5 ; UGT1A10 ; LOC100286922 ; UGT1A4 ; UGT1A9 ; UGT1A8 ; UGT1A3			2	233755003	splice region variant	C/G;T	snv	0.48		2
rs12988520	UGT1A6 ; UGT1A9 ; UGT1A8 ; UGT1A10 ; UGT1A7	1.000	0.040	2	233698748	intron variant	A/C	snv		0.51	2
rs10929302	UGT1A7 ; UGT1A9 ; UGT1A5 ; UGT1A8 ; UGT1A3 ; UGT1A6 ; UGT1A10 ; LOC100286922 ; UGT1A4			2	233757136	intron variant	G/A	snv		0.30	2
rs11673726	UGT1A8 ; LOC100286922 ; UGT1A7 ; UGT1A6 ; UGT1A3 ; UGT1A10 ; UGT1A5 ; UGT1A9 ; UGT1A4			2	233755414	non coding transcript exon variant	G/A;T	snv			2