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
rs10510554	RARB			3	25058285	intron variant	T/C	snv		0.53	2
rs10968577	LINGO2			9	28415514	intron variant	C/T	snv		0.27	3
rs11209951	LOC105378797			1	72371807	intron variant	C/T	snv		0.61	3
rs11672660	GIPR ; MIR642B			19	45676926	intron variant	C/T	snv	0.18	0.17	5
rs12429545				13	53528071	intron variant	G/A;T	snv		0.12	4
rs1308362	MRAS			3	138385085	intron variant	A/G;T	snv			2
rs13191362	PRKN			6	162612318	intron variant	A/G	snv		8.7E-02	3
rs1569980	LOC102724934			14	29215315	intron variant	T/C	snv		0.75	2
rs17024393	GNAT2			1	109612066	intron variant	T/C	snv		4.6E-02	4
rs1720825	MRAS			3	138389241	intron variant	A/G;T	snv			2
rs17381664	ZZZ3	1.000	0.080	1	77582646	intron variant	T/C	snv		0.29	3
rs1934100				9	23234310	intron variant	A/T	snv		0.45	2
rs1998710	LINC01720			1	190701754	intron variant	C/T	snv		0.57	2
rs2030323	BDNF	0.925	0.080	11	27706992	intron variant	A/C	snv		0.83	6
rs2033529	TDRG1			6	40380914	intron variant	A/C;G	snv			4
rs2035935	RASA2			3	141587171	intron variant	A/G;T	snv			2
rs2044148	NCOA1			2	24514964	intron variant	G/A	snv		0.15	2
rs2049045	BDNF-AS ; BDNF	1.000	0.080	11	27672694	intron variant	G/A;C	snv		0.13	3
rs2241423	MAP2K5	0.882	0.120	15	67794500	intron variant	G/A	snv		0.29	7
rs2303108	ZC3H4			19	47086638	intron variant	T/C	snv		0.63	3
rs2365389	FHIT			3	61250788	intron variant	C/T	snv		0.56	3
rs2371767	ADAMTS9-AS2			3	64732582	intron variant	G/C	snv		0.38	5
rs2395607	UHRF1BP1			6	34805950	intron variant	C/T	snv		0.22	2
rs2590838	PBRM1			3	52588070	intron variant	G/A	snv		0.55	3
rs2710323	ITIH1	0.851	0.080	3	52781889	intron variant	T/C	snv	0.49	0.54	7