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
rs4727027	ZNF398			7	149172185	intron variant	G/A;C	snv			2
rs12413946	ZNF365			10	62671446	non coding transcript exon variant	T/C	snv		6.2E-02	2
rs10852622	ZFPM1			16	88490472	intron variant	A/G	snv		0.35	2
rs5758297	ZC3H7B			22	41324693	intron variant	A/G	snv		0.41	2
rs238914	ZBTB16			11	114113387	intron variant	C/A	snv		0.45	5
rs2846630	ZBTB16			11	114086475	intron variant	G/A	snv		0.35	5
rs55905691	WDR36			5	111090287	intron variant	A/G	snv		0.13	2
rs79881201	WDR36			5	111092097	5 prime UTR variant	C/T	snv		0.26	2
rs11654074	VMP1			17	59748211	intron variant	A/C	snv		0.40	5
rs13007211	VAMP8			2	85573959	intron variant	A/T	snv		0.31	2
rs9900933	UNK			17	75805073	intron variant	T/A;C;G	snv			3
rs2182885	UBAC2			13	99202870	intron variant	G/A	snv		0.46	2
rs4837892	TTLL11			9	121826025	intron variant	G/T	snv		0.36	13
rs734095	TSPAN32 ; C11orf21			11	2301968	5 prime UTR variant	C/G;T	snv			2
rs61612642	TRERF1			6	42229969	intron variant	C/T	snv		0.21	2
rs6500550	TRAP1			16	3696240	intron variant	C/G;T	snv			5
rs2856451	TNXB			6	32043581	intron variant	A/G;T	snv	0.59		3
rs834603	TNS3			7	47408324	intron variant	A/G	snv		0.47	4
rs960709	TNIP1	0.882	0.120	5	151081488	intron variant	A/G;T	snv			4
rs3181348	TNFSF8 ; DELEC1			9	114931904	intron variant	G/A;C	snv			2
rs7834745	TNFRSF11B			8	118927620	intron variant	A/G	snv		0.18	2
rs12550612	TNFRSF10C			8	23109256	intron variant	G/A	snv		0.83	5
rs78487399	THADA			2	43582208	intron variant	G/C	snv		6.2E-02	5
rs7705526	TERT	0.776	0.240	5	1285859	intron variant	C/A;T	snv			15
rs3809627	TBX6 ; YPEL3			16	30091839	5 prime UTR variant	C/A	snv		0.41	5