DisGeNET - a database of gene-disease associations

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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
rs66461782	ZRANB2-AS1 ; ZRANB2 ; MIR186			1	71067604	intron variant	A/T	snv	0.32	0.27	2
rs10980926	ZNF483			9	111531354	intron variant	A/G	snv		0.56	2
rs10217747	ZNF483			9	111547655	3 prime UTR variant	T/A;C	snv			1
rs10441737	ZNF483			9	111539305	intron variant	C/T	snv		0.59	1
rs7873730	ZNF483			9	111541399	intron variant	A/T	snv		0.11	1
rs882609	ZNF446 ; SLC27A5			19	58480112	3 prime UTR variant	G/A;T	snv			1
rs61744130	ZNF331			19	53576813	missense variant	T/C	snv	5.9E-02	3.9E-02	1
rs1532331	ZNF131			5	43116728	intron variant	G/T	snv		0.70	1
rs7007681	ZFHX4			8	76783308	intron variant	G/A	snv		0.28	1
rs7821604	ZFHX4			8	76763076	intron variant	C/G;T	snv			1
rs11556924	ZC3HC1	0.752	0.240	7	130023656	missense variant	C/A;T	snv	4.0E-06; 0.28		21
rs3810291	ZC3H4			19	47065746	3 prime UTR variant	G/A	snv		0.50	9
rs6010651	ZBTB46			20	63786890	intron variant	A/C	snv		0.43	1
rs7643617	ZBTB20			3	115034231	intron variant	A/C;T	snv			1
rs2425670	YWHAB			20	44893088	intron variant	G/A	snv		0.61	1
rs2067082	XYLB			3	38396691	intron variant	G/C	snv		0.44	1
rs12926791	WWP2			16	69815643	intron variant	C/A;G;T	snv			1
rs78352137	WDR25			14	100454079	intron variant	T/C	snv		7.7E-02	2
rs10144321	WDR25			14	100416068	intron variant	A/G	snv		0.24	1
rs12894936	WDR25			14	100380654	intron variant	T/C	snv		0.55	1
rs13068899	VGLL3			3	86895788	intron variant	A/T	snv		0.56	1
rs139309976	VAC14			16	70751506	intron variant	G/A	snv		5.5E-03	1
rs2254479	USP49			6	41863405	intron variant	G/A	snv		0.62	2
rs2256464	USP35			11	78206259	intron variant	C/A	snv		0.28	1
rs4353638	USP34			2	61271884	intron variant	A/G	snv		0.14	1