DisGeNET - a database of gene-disease associations

Source: GWASDB

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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
rs11166389	SLC35A3 ; RNU6-1318P	1.000	0.040	1	100000723	non coding transcript exon variant	G/A	snv		0.15	2
rs1014290	SLC2A9 ; LOC105374476	0.827	0.280	4	10000237	intron variant	G/A	snv		0.72	3
rs2403261	SBF2			11	10000244	non coding transcript exon variant	T/C	snv		0.25	1
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
rs7006527	RGS22	0.851	0.040	8	100012277	intron variant	A/C;T	snv			1
rs4107019	GRIN2A	1.000	0.080	16	10001342	intron variant	T/C	snv		9.6E-02	1
rs4622999	SLC2A9 ; LOC105374476	0.925	0.120	4	10001771	intron variant	C/G	snv		0.46	3
rs6963345	ZKSCAN1			7	100020983	intron variant	G/A;C	snv			1
rs7657096	SLC2A9 ; LOC105374476	0.925	0.120	4	10002376	intron variant	A/G	snv		0.13	2
rs545854		0.882	0.160	8	10002570	intron variant	G/C	snv		0.85	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
rs7932484	SBF2			11	10003336	intron variant	T/C	snv		0.27	1
rs10883437		1.000	0.040	10	100035604	regulatory region variant	T/A;G	snv		0.43	2
rs6853437	SLC2A9 ; LOC105374476	0.925	0.120	4	10003811	intron variant	G/A	snv		0.72	3
rs11599750	CPN1			10	100045685	intron variant	C/T	snv		0.40	1
rs10022499	LOC105374476 ; SLC2A9	0.925	0.120	4	10004913	intron variant	C/A	snv		0.72	3
rs7084921	CPN1			10	100054045	intron variant	C/T	snv		0.44	1
rs9291640	SLC2A9 ; LOC105374476	0.925	0.120	4	10005462	intron variant	C/T	snv		0.72	3
rs10209110	AFF3	1.000	0.120	2	100056230	intron variant	C/T	snv		0.47	1
rs9291642	SLC2A9 ; LOC105374476	0.925	0.120	4	10005651	intron variant	C/G;T	snv			3
rs3755955	IDUA	0.925	0.080	4	1000626	missense variant	G/A;C	snv	0.16; 8.0E-06		1
rs2896514	SBF2			11	10006354	intron variant	T/C	snv		0.25	1
rs3796840	SLC2A9 ; LOC105374476	0.925	0.120	4	10006497	non coding transcript exon variant	C/T	snv		6.1E-02	2