DisGeNET - a database of gene-disease associations

List of associated variants

Arthritis, Gouty, C0003868

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
rs1014290	SLC2A9 ; LOC105374476	0.827	0.280	4	10000237	intron variant	G/A	snv		0.72	6
rs7696895	LOC105374476 ; SLC2A9	0.925	0.120	4	10000801	intron variant	T/C	snv		0.24	3
rs9991278	SLC2A9 ; LOC105374476	0.925	0.120	4	10001041	intron variant	T/A;C	snv			3
rs4622999	SLC2A9 ; LOC105374476	0.925	0.120	4	10001771	intron variant	C/G	snv		0.46	3
rs7657096	SLC2A9 ; LOC105374476	0.925	0.120	4	10002376	intron variant	A/G	snv		0.13	2
rs17247314	SLC2A9 ; LOC105374476	0.925	0.120	4	10003119	intron variant	C/G	snv		0.43	3
rs10023068	LOC105374476 ; SLC2A9	0.925	0.120	4	10003208	intron variant	A/G	snv		0.72	3
rs6853437	SLC2A9 ; LOC105374476	0.925	0.120	4	10003811	intron variant	G/A	snv		0.72	3
rs10022499	LOC105374476 ; SLC2A9	0.925	0.120	4	10004913	intron variant	C/A	snv		0.72	3
rs9291640	SLC2A9 ; LOC105374476	0.925	0.120	4	10005462	intron variant	C/T	snv		0.72	3
rs9291642	SLC2A9 ; LOC105374476	0.925	0.120	4	10005651	intron variant	C/G;T	snv			3
rs3796840	SLC2A9 ; LOC105374476	0.925	0.120	4	10006497	non coding transcript exon variant	C/T	snv		6.1E-02	2
rs4543113	LOC105374476 ; SLC2A9	0.925	0.120	4	10006681	non coding transcript exon variant	G/A;C	snv			3
rs6845554	LOC105374476 ; SLC2A9	0.925	0.120	4	10011549	intron variant	T/G	snv		0.55	3
rs3756236	SLC2A9 ; LOC105374476	0.925	0.120	4	10011839	intron variant	T/A;G	snv			3
rs6827754	SLC2A9 ; LOC105374476	0.925	0.120	4	10016529	intron variant	C/A;G;T	snv			3
rs13128385	SLC2A9	0.925	0.120	4	10017939	intron variant	C/G	snv		3.8E-02	2
rs13133766	SLC2A9	0.925	0.120	4	10018108	intron variant	C/T	snv		0.44	3
rs3775942	SLC2A9	0.925	0.120	4	10018683	intron variant	G/A	snv		9.8E-02	2
rs2240720	SLC2A9	0.925	0.120	4	10018856	intron variant	C/T	snv		0.44	3
rs2240721	SLC2A9	0.925	0.120	4	10018940	intron variant	G/A	snv	0.52	0.44	3
rs2240723	SLC2A9	0.925	0.120	4	10019527	intron variant	G/A	snv		9.9E-02	2
rs2240724	SLC2A9	0.925	0.120	4	10019666	intron variant	G/C	snv		0.44	3
rs13122112	SLC2A9	0.925	0.120	4	10019780	intron variant	G/A	snv		9.9E-02	2
rs6849273	SLC2A9	0.925	0.120	4	10019971	intron variant	C/G;T	snv			3