DisGeNET - a database of gene-disease associations

List of associated variants

Glioma, C0017638

Source: ALL

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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
rs4636162	CCDC26	1.000	0.040	8	129627294	non coding transcript exon variant	G/A	snv		0.30	1
rs6985166	CCDC26	1.000	0.040	8	129666930	intron variant	A/G	snv		0.34	1
rs9656979	CCDC26	1.000	0.040	8	129652161	intron variant	T/C	snv		0.37	1
rs603965	CCND1	0.732	0.440	11	69648142	splice region variant	G/A	snv			14
rs147960238	CD163	1.000	0.040	12	7485786	intron variant	T/C	snv		8.3E-03	1
rs3212986	CD3EAP ; ERCC1	0.620	0.400	19	45409478	stop gained	C/A;G;T	snv	0.29; 4.3E-06; 4.3E-06		42
rs753152604	CDK4	0.827	0.040	12	57751680	missense variant	C/A	snv			7
rs104894104	CDKN2A	0.790	0.160	9	21971019	missense variant	G/A;T	snv			7
rs4977574	CDKN2B-AS1	0.695	0.520	9	22098575	intron variant	A/G;T	snv			26
rs4977756	CDKN2B-AS1	0.683	0.440	9	22068653	intron variant	G/A	snv		0.64	24
rs2383207	CDKN2B-AS1	0.695	0.280	9	22115960	intron variant	A/G	snv		0.64	22
rs2157719	CDKN2B-AS1	0.708	0.360	9	22033367	non coding transcript exon variant	C/T	snv		0.71	17
rs2151280	CDKN2B-AS1	0.701	0.360	9	22034720	non coding transcript exon variant	G/A	snv		0.46	16
rs1412829	CDKN2B-AS1	0.742	0.400	9	22043927	intron variant	A/G	snv		0.28	14
rs10116277	CDKN2B-AS1	0.827	0.160	9	22081398	intron variant	G/T	snv		0.62	8
rs10120688	CDKN2B-AS1	0.807	0.080	9	22056500	intron variant	G/A	snv		0.50	7
rs7049105	CDKN2B-AS1	0.807	0.120	9	22028802	intron variant	A/G	snv		0.58	7
rs1537375	CDKN2B-AS1	0.882	0.120	9	22116072	intron variant	T/C;G	snv			6
rs634537	CDKN2B-AS1	0.851	0.080	9	22032153	intron variant	T/G	snv		0.28	6
rs944797	CDKN2B-AS1	0.882	0.120	9	22115287	intron variant	T/C;G	snv		0.49	5
rs145929329	CDKN2B-AS1	0.882	0.040	9	22066213	intron variant	TTTT/-;T;TT;TTT;TTTTT;TTTTTT;TTTTTTTTTT	delins		0.58	3
rs573687	CDKN2B-AS1	0.882	0.120	9	22011643	intron variant	G/A	snv		0.26	3
rs1412832	CDKN2B-AS1	0.925	0.080	9	22077544	intron variant	C/T	snv		0.78	2
rs1444669684	CDKN2B-AS1 ; CDKN2A	0.658	0.480	9	21994285	missense variant	C/A;T	snv			36
rs3217992	CDKN2B-AS1 ; CDKN2B	0.683	0.480	9	22003224	3 prime UTR variant	C/T	snv		0.32	22