DisGeNET - a database of gene-disease associations

Source: ALL

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
rs964184	ZPR1	0.716	0.440	11	116778201	3 prime UTR variant	G/C	snv		0.82	47
rs143012756	ZNRF3			22	28914537	intron variant	G/A	snv		3.2E-03	2
rs2306589	ZNHIT3			17	36493030	non coding transcript exon variant	T/C	snv		0.49	3
rs112134552	ZNF853			7	6619030	intron variant	G/A	snv		9.5E-02	2
rs28729203	ZNF800			7	127391863	intron variant	G/A;C;T	snv			2
rs12406643	ZNF691			1	42845892	intron variant	A/G	snv		0.16	2
rs863750	ZNF664-RFLNA ; RFLNA			12	124020897	intron variant	C/T	snv		0.53	7
rs11665661	ZNF611			19	52725740	intron variant	T/C	snv		0.71	2
rs4375747	ZNF516			18	76359827	3 prime UTR variant	C/T	snv		5.2E-02	2
rs8088980	ZNF407	1.000	0.040	18	74666435	intron variant	C/T	snv		0.51	3
rs4811444	ZNF217			20	53590524	intron variant	T/C	snv		0.31	2
rs571658566	ZNF211			19	57632578	intron variant	G/A;T	snv			2
rs7080849	ZMIZ1-AS1			10	79041217	intron variant	T/A;C;G	snv			2
rs142529006	ZKSCAN1			7	100022093	intron variant	T/A	snv		6.9E-03	4
rs28609654	ZFYVE1			14	72989530	intron variant	T/C	snv		0.11	2
rs11774829	ZFPM2			8	104966140	intron variant	T/A	snv		7.6E-02	3
rs74035509	ZFPM1			16	88500925	intron variant	C/T	snv		0.10	5
rs927292	ZFP36L1	1.000	0.120	14	68792124	intron variant	C/G	snv		0.68	3
rs191719058	ZFAND4			10	45654497	intron variant	T/C	snv		1.3E-02	2
rs2180414	ZDHHC14			6	157461755	intron variant	C/A;G	snv			2
rs77786029	ZCCHC8			12	122496512	intron variant	C/T	snv		2.9E-02	2
rs11556924	ZC3HC1	0.752	0.240	7	130023656	missense variant	C/A;T	snv	4.0E-06; 0.28		21
rs9607793	ZC3H7B			22	41340086	missense variant	G/A	snv	1.3E-02	1.3E-02	2
rs12973221	ZC3H4			19	47111403	intron variant	C/A	snv		7.6E-02	2
rs61827266	ZC3H11A ; ZBED6			1	203825625	intron variant	G/A	snv		0.12	2