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
rs8070737	ZZEF1			17	4077772	intron variant	G/T	snv		0.14	1
rs9896963	ZZEF1			17	4063297	intron variant	T/C;G	snv			1
rs4823006	ZNRF3			22	29055683	3 prime UTR variant	A/G	snv		0.41	5
rs2294239	ZNRF3			22	29053489	intron variant	A/G	snv		0.36	4
rs2179129	ZNRF3			22	29054935	3 prime UTR variant	A/G	snv		0.34	2
rs115770674	ZNRF3			22	28860678	intergenic variant	G/A	snv		6.3E-02	1
rs2306589	ZNHIT3			17	36493030	non coding transcript exon variant	T/C	snv		0.49	3
rs863750	ZNF664-RFLNA ; RFLNA			12	124020897	intron variant	C/T	snv		0.53	7
rs11057450	ZNF664-RFLNA ; RFLNA			12	124100790	intron variant	G/A	snv		0.28	1
rs11057553	ZNF664-RFLNA ; RFLNA			12	124267534	intron variant	C/T	snv		3.9E-02	1
rs2547049	ZNF568			19	36991915	intron variant	G/A	snv		0.54	1
rs2047937	ZNF423	0.925	0.120	16	49830880	intron variant	C/T	snv		0.50	5
rs34050011	ZNF423			16	49834602	intron variant	C/A	snv		0.40	1
rs12828318	ZNF268			12	133189536	intron variant	A/G	snv		0.14	1
rs36127550	ZNF268			12	133203723	missense variant	G/A;T	snv	0.17		1
rs559986	ZMYM4			1	35375657	intron variant	C/T	snv		0.33	1
rs6480914	ZMIZ1-AS1			10	79012834	intron variant	G/A	snv		0.63	1
rs779933	ZMIZ1			10	79158760	intron variant	G/A	snv		0.36	2
rs780159	ZMIZ1			10	79147390	intron variant	A/C;G	snv			2
rs703984	ZMIZ1			10	79181660	intron variant	G/C;T	snv			1
rs4812492	ZHX3			20	41309482	intron variant	T/C	snv		0.66	1
rs7821292	ZFAT			8	134698105	intron variant	C/T	snv		0.39	1
rs10988105	ZDHHC12			9	128722247	intron variant	C/T	snv		0.39	1
rs4705986	ZCCHC10			5	133013962	intron variant	T/G	snv		3.8E-02	1
rs905938	ZBTB7B ; DCST2			1	155018913	intron variant	T/C	snv		0.24	5