DisGeNET - a database of gene-disease associations

Source: GWASCAT ×

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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
rs71559067	ZSCAN16-AS1			6	28026638	intron variant	A/T	snv		5.0E-02	1
rs2634675	ZNF641			12	48347072	intron variant	A/G	snv		0.40	1
rs2732481	ZNF641			12	48343202	missense variant	T/A;G	snv	4.0E-06; 0.28		1
rs111827672	ZNF585A			19	37158964	intron variant	T/A	snv		0.24	1
rs78241494	ZNF585A			19	37158846	intron variant	T/C	snv		0.24	1
rs4525087	ZNF436			1	23365736	intron variant	A/C	snv		0.58	1
rs7759001	ZNF391 ; ZNF204P			6	27373630	upstream gene variant	G/A;C	snv			2
rs77915916	ZNF318			6	43319984	intron variant	A/T	snv		5.9E-02	2
rs57126710	ZNF260			19	36526731	intron variant	C/T	snv		0.28	1
rs131263	ZMAT5			22	29737056	intron variant	C/T	snv		0.32	1
rs2261092	ZGPAT			20	63722581	intron variant	A/G	snv		0.95	1
rs113445505	ZFP30			19	37667068	intron variant	C/T	snv		0.26	1
rs1858800	ZFHX3	1.000	0.120	16	72990377	intron variant	C/T	snv		0.28	2
rs78614739	ZDHHC18			1	26847689	intron variant	C/T	snv		0.14	1
rs6440003	ZBTB38			3	141375367	intron variant	G/A	snv		0.54	3
rs7624084	ZBTB38			3	141374443	intron variant	T/C	snv		0.54	2
rs28470843	YY1 ; MIR6764			14	100276321	non coding transcript exon variant	T/A;C	snv			1
rs7429308	XYLB			3	38437984	regulatory region variant	T/C;G	snv			1
rs10096421	XKR6			8	10974358	intron variant	T/G	snv		0.60	1
rs11783418	XKR6			8	10984348	intron variant	G/A;T	snv			1
rs56140069	WWP2			16	69761420	upstream gene variant	A/T	snv		0.12	1
rs62050038	WWP2			16	69768962	intron variant	A/T	snv		0.12	1
rs199592697	WNT7A			3	13854632	missense variant	C/T	snv	1.7E-04	1.1E-04	3
rs6795744	WNT7A			3	13865353	intron variant	G/A	snv		0.16	2
rs883541	WIPI1 ; PRKAR1A			17	68452981	missense variant	G/A	snv	0.74	0.78	1