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
rs1000879	VIL1			2	218439407	intron variant	G/A	snv		4.1E-02	3
rs10019888				4	26061368	regulatory region variant	A/G	snv		0.17	3
rs10096633		1.000	0.040	8	19973410	regulatory region variant	C/T	snv		0.22	8
rs10099160	LPL			8	19964304	intron variant	T/G	snv		0.20	2
rs10107815	MSRA			8	10156645	intron variant	G/C	snv		5.1E-02	4
rs10120087	ABCA1			9	104898869	intron variant	C/A;T	snv			2
rs10120653	RXRA			9	134415237	intron variant	G/T	snv		1.2E-02	3
rs10149080	GCH1			14	54889676	intron variant	C/T	snv		4.4E-02	2
rs10200587	BMPR2			2	202554561	intron variant	A/G	snv		7.0E-03	2
rs10212938	LOC107986321 ; NPY2R			4	155207180	non coding transcript exon variant	T/C	snv		2.6E-02	2
rs102275	TMEM258	0.827	0.320	11	61790331	non coding transcript exon variant	T/C	snv		0.47	18
rs10239940	BAZ1B			7	73487060	intron variant	A/T	snv		2.6E-02	2
rs10271556	NAMPT			7	106258428	intron variant	C/T	snv		5.6E-02	4
rs10305650	ARNT			1	150876501	intron variant	G/A;C	snv	1.3E-02		2
rs10305685	ARNT			1	150838529	intron variant	T/C	snv		5.4E-02	2
rs1031045	LPL			8	19943601	intron variant	G/A	snv		0.12	3
rs103294		0.827	0.200	19	54293995	downstream gene variant	T/C	snv		0.82	7
rs10402729	NCAN			19	19244291	intron variant	T/C	snv		3.3E-02	4
rs10405178	SLC25A42			19	19064943	intron variant	T/G	snv		2.5E-02	2
rs10411413	SUGP2			19	19009572	intron variant	C/T	snv		2.4E-02	2
rs1042034	APOB	0.851	0.240	2	21002409	missense variant	C/T	snv	0.70	0.78	15
rs10422058	ARMC6			19	19047391	intron variant	T/A;C	snv			2
rs10427943	CABIN1			22	24131331	intron variant	G/T	snv		1.2E-02	2
rs10468017	ALDH1A2	0.851	0.120	15	58386313	intron variant	C/T	snv		0.24	12
rs10478730	EDN1			6	12297276	downstream gene variant	C/T	snv		1.2E-02	5