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
rs4887991	WWOX			16	78887166	intron variant	A/C;G	snv			1
rs11613704	WNK1			12	871759	intron variant	C/A;T	snv			1
rs113400434	WDR59			16	74983615	intron variant	G/A	snv		2.5E-02	1
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
rs10045577	WDR36			5	111090753	intron variant	C/A;G;T	snv			1
rs2416257	WDR36	0.882	0.160	5	111099792	intron variant	C/G;T	snv			1
rs133342	WBP2NL			22	42022906	intron variant	G/C;T	snv			1
rs11654074	VMP1			17	59748211	intron variant	A/C	snv		0.40	5
rs55860526	VLDLR-AS1			9	2602279	intron variant	T/C	snv		0.20	1
rs2228570	VDR	0.521	0.760	12	47879112	start lost	A/C;G;T	snv	0.63		1
rs17484960	VAV3			1	107794486	intron variant	G/A	snv		0.48	1
rs13007211	VAMP8			2	85573959	intron variant	A/T	snv		0.31	2
rs141361914	USP7			16	8941610	intron variant	C/T	snv		4.6E-02	1
rs3131610	USP50 ; USP8			15	50507898	3 prime UTR variant	G/A	snv		0.25	4
rs9900933	UNK			17	75805073	intron variant	T/A;C;G	snv			3
rs1071849	UBXN11 ; CD52			1	26320235	missense variant	A/G	snv	0.67	0.70	1
rs4299301	UBE2E3			2	180982678	intron variant	A/T	snv		0.58	1
rs12483051	UBASH3A			21	42430604	intron variant	C/G;T	snv			1
rs2182885	UBAC2			13	99202870	intron variant	G/A	snv		0.46	2
rs912131	UBAC2			13	99380092	intron variant	A/G	snv		0.57	2
rs7332672	UBAC2			13	99225217	intron variant	C/T	snv		0.46	1
rs112069438	TXNDC11			16	11733034	intron variant	G/A	snv		2.1E-02	1
rs4047777	TUBD1			17	59882526	intron variant	A/T	snv		0.27	1
rs4837892	TTLL11			9	121826025	intron variant	G/T	snv		0.36	13