DisGeNET - a database of gene-disease associations

List of shared variants

Hyperuricemia, C0740394

Disease: Gout

Source: ALL

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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
rs11231825	SLC22A12	0.827	0.240	11	64592802	synonymous variant	T/C	snv	0.57	0.51	5
rs16890979	SLC2A9	0.827	0.200	4	9920543	missense variant	C/T	snv	0.24	0.29	7
rs2054576	ABCG2	0.882	0.160	4	88107623	intron variant	A/G	snv		7.8E-02	4
rs2231142	ABCG2	0.583	0.680	4	88131171	missense variant	G/C;T	snv	4.0E-06; 0.12		56
rs2941484	HNF4G	0.882	0.160	8	75566533	3 prime UTR variant	C/T	snv		0.52	4
rs3825016	SLC22A12	0.882	0.160	11	64591814	synonymous variant	C/T	snv	0.57	0.51	3
rs475688	SLC22A12	0.882	0.160	11	64596819	intron variant	C/T	snv		0.25	3
rs505802	SLC22A12	0.882	0.160	11	64589600	upstream gene variant	T/C	snv		0.45	4
rs671	ALDH2	0.529	0.840	12	111803962	missense variant	G/A	snv	1.9E-02	5.8E-03	116
rs6837293	PRKG2	0.925	0.160	4	81141777	intron variant	C/A;T	snv			2
rs6855911	SLC2A9	0.851	0.200	4	9934286	intron variant	A/G	snv		0.33	7
rs7688672	PRKG2	0.925	0.160	4	81148295	intron variant	G/A	snv		0.39	2
rs7903456	SHLD2	0.882	0.160	10	87159562	intron variant	C/T	snv		0.69	3
rs893006	SLC22A12	0.882	0.160	11	64598324	intron variant	C/A	snv		0.61	3