DisGeNET - a database of gene-disease associations

Source: ALL

Variants associated to the Disease: Uric acid measurement (procedure) ×

Variants associated to the Gene: SLC2A9 ×

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
rs16890979	SLC2A9	0.827	0.200	4	9920543	missense variant	C/T	snv	0.24	0.29	7
rs6855911	SLC2A9	0.851	0.200	4	9934286	intron variant	A/G	snv		0.33	7
rs734553	SLC2A9	0.851	0.240	4	9921380	intron variant	G/A;T	snv			7
rs737267	SLC2A9	0.851	0.240	4	9933120	intron variant	G/A;T	snv			7
rs6449213	SLC2A9 ; LOC105374476	0.827	0.240	4	9992591	intron variant	C/T	snv		0.82	7
rs11722228	SLC2A9	0.851	0.160	4	9914117	intron variant	C/T	snv		0.32	6
rs1014290	SLC2A9 ; LOC105374476	0.827	0.280	4	10000237	intron variant	G/A	snv		0.72	6
rs13129697	SLC2A9	0.925	0.120	4	9925343	intron variant	T/G	snv		0.39	5
rs149454410	SLC2A9	0.925	0.120	4	9942000	missense variant	C/G;T	snv	4.0E-05; 3.2E-04		5
rs4481233	SLC2A9	0.925	0.120	4	9954455	intron variant	C/T	snv		0.16	5
rs733175	SLC2A9	0.851	0.240	4	10048517	intron variant	C/T	snv		0.77	5
rs7442295	SLC2A9	0.925	0.120	4	9964756	intron variant	A/G	snv		0.28	5
rs7660895	SLC2A9	0.882	0.200	4	9983821	intron variant	A/G;T	snv			5
rs3775948	LOC105374476 ; SLC2A9	0.882	0.160	4	9993558	intron variant	G/A;C	snv			4
rs11942223	SLC2A9	0.882	0.160	4	9961141	intron variant	T/C	snv		0.28	4
rs7671266	SLC2A9	0.925	0.120	4	10054752	intron variant	T/C	snv		0.73	4
rs13111638	SLC2A9 ; LOC105374476	0.882	0.200	4	9995266	intron variant	T/C	snv		0.82	4
rs10011206	LOC105374476 ; SLC2A9	0.925	0.120	4	9990331	intron variant	C/T	snv		0.23	3
rs10022499	LOC105374476 ; SLC2A9	0.925	0.120	4	10004913	intron variant	C/A	snv		0.72	3
rs10023068	LOC105374476 ; SLC2A9	0.925	0.120	4	10003208	intron variant	A/G	snv		0.72	3
rs10939650	LOC105374476 ; SLC2A9	0.925	0.120	4	9996816	synonymous variant	C/G;T	snv	1.2E-05; 0.70		3
rs17187075	LOC105374476 ; SLC2A9	0.925	0.120	4	9988704	intron variant	G/C	snv		0.45	3
rs3796842	LOC105374476 ; SLC2A9	0.925	0.120	4	9994227	intron variant	A/T	snv		0.48	3
rs4385059	LOC105374476 ; SLC2A9	0.925	0.120	4	9987609	intron variant	C/T	snv		0.84	3
rs4543113	LOC105374476 ; SLC2A9	0.925	0.120	4	10006681	non coding transcript exon variant	G/A;C	snv			3