DisGeNET - a database of gene-disease associations

Source: GWASCAT ×

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
rs4823006	ZNRF3			22	29055683	3 prime UTR variant	A/G	snv		0.41	5
rs5762862	ZNRF3			22	28856744	intergenic variant	G/A;T	snv			3
rs6015450	ZNF831			20	59176062	intron variant	A/G	snv		0.14	4
rs6026740	ZNF831			20	59165293	intron variant	A/G	snv		0.15	3
rs12940887	ZNF652			17	49325445	intron variant	C/T	snv		0.28	3
rs10948071	ZNF318			6	43312975	intron variant	C/T	snv		0.46	4
rs1563788	ZNF318			6	43340625	intron variant	C/T	snv		0.42	4
rs8098380	YES1			18	721563	downstream gene variant	A/C	snv		0.33	4
rs17622152	YEATS2			3	183802324	non coding transcript exon variant	G/A	snv		0.26	3
rs10776752	WNT2B			1	112501706	intron variant	G/T	snv		8.8E-02	4
rs3790604	WNT2B			1	112504257	intron variant	C/A	snv		7.8E-02	5
rs284844	WBP1L			10	102794772	intron variant	A/G	snv		0.82	3
rs2286525	TBX2-AS1			17	61394762	intron variant	G/A	snv		0.73	3
rs2240736	TBX2			17	61408032	non coding transcript exon variant	C/T	snv	0.64	0.68	4
rs8068318	TBX2			17	61406405	non coding transcript exon variant	C/T	snv		0.56	5
rs2649044	SWAP70			11	9742422	intron variant	C/T	snv		0.55	4
rs4910498	SWAP70			11	9743956	intron variant	A/T	snv		0.61	4
rs12118370	ST7L			1	112605645	intron variant	A/G	snv		0.24	3
rs6658555	ST7L			1	112555912	missense variant	C/T	snv	0.19	0.20	2
rs13107325	SLC39A8	0.776	0.520	4	102267552	missense variant	C/A;T	snv	4.0E-06; 4.5E-02		24
rs2270860	SLC22A7 ; CRIP3			6	43302413	splice region variant	C/T	snv	0.37	0.43	4
rs16896398	SLC22A7			6	43294966	upstream gene variant	A/T	snv		0.42	5
rs2306363	SIPA1			11	65638129	5 prime UTR variant	G/T	snv		0.15	7
rs7310615	SH2B3	0.882		12	111427245	intron variant	C/G	snv		0.67	12
rs167479	RGL3			19	11416089	missense variant	T/A;C;G	snv			5