DisGeNET - a database of gene-disease associations

Source: ALL

Variants associated to the Gene: MTAP ×

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
rs7023329	MTAP	0.790	0.160	9	21816529	intron variant	A/G	snv		0.50	9
rs10118757	MTAP	0.827	0.120	9	21853340	intron variant	A/G	snv		0.26	7
rs869329	MTAP	0.851	0.080	9	21804694	intron variant	A/G;T	snv			4
rs10757257	MTAP	0.882	0.080	9	21806565	intron variant	G/A	snv		0.34	3
rs11532907	MTAP	0.882	0.080	9	21844773	intron variant	A/G;T	snv			3
rs7023954	MTAP	0.925	0.040	9	21816759	missense variant	G/A	snv	0.40	0.42	2
rs7027989	MTAP	0.925	0.120	9	21817755	intron variant	A/G;T	snv			2
rs869330	MTAP	0.925	0.080	9	21804618	intron variant	A/G	snv		0.62	2
rs10811625	MTAP	1.000	0.040	9	21826841	intron variant	G/A;T	snv			1
rs10965144	MTAP	1.000	0.040	9	21808914	5 prime UTR variant	C/T	snv		0.36	1
rs185224597	MTAP			9	21860064	non coding transcript exon variant	C/T	snv		3.2E-03	1
rs201131773	MTAP	1.000	0.040	9	21805207	intron variant	-/AC	delins			1
rs3900787	MTAP	1.000	0.040	9	21828111	intron variant	A/C;T	snv			1
rs3922992	MTAP	1.000	0.040	9	21827407	intron variant	A/G	snv		0.34	1
rs3927737	MTAP	1.000	0.040	9	21827993	intron variant	G/A;C	snv			1
rs4364717	MTAP			9	21801531	upstream gene variant	A/G	snv		0.55	1
rs67134687	MTAP	1.000		9	21845309	intron variant	A/G	snv		9.2E-02	1
rs7851133	MTAP			9	21846328	intron variant	C/T	snv		0.24	1
rs885518	MTAP	1.000	0.040	9	21830158	intron variant	A/G	snv		0.17	1