DisGeNET - a database of gene-disease associations

List of associated variants

Glioblastoma Multiforme, C1621958

Source: BEFREE ×

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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
rs1259560536	ADAM33	1.000	0.040	20	3671756	missense variant	T/C	snv		7.0E-06	1
rs145929329	CDKN2B-AS1	0.882	0.040	9	22066213	intron variant	TTTT/-;T;TT;TTT;TTTTT;TTTTTT;TTTTTTTTTT	delins		0.58	1
rs634537	CDKN2B-AS1	0.851	0.080	9	22032153	intron variant	T/G	snv		0.28	1
rs6062302	RTEL1 ; RTEL1-TNFRSF6B	0.882	0.040	20	63689615	synonymous variant	T/C	snv	0.74	0.81	1
rs2291427	ALOX5	0.925	0.040	10	45440776	intron variant	A/G;T	snv			2
rs11548193	BCAT2	0.925	0.040	19	48799813	missense variant	G/A;C	snv	0.14		2
rs11670188	BTBD2	0.925	0.040	19	2014038	non coding transcript exon variant	A/G	snv		0.16	2
rs10464870	CCDC26	0.882	0.040	8	129465577	intron variant	C/T	snv		0.80	2
rs1210653597	CDKN2A	0.925	0.120	9	21968756	missense variant	T/C	snv			2
rs11979158	EGFR	0.882	0.040	7	55091656	intron variant	A/G;T	snv		0.20	2
rs9642393	EGFR	0.925	0.040	7	55177954	intron variant	T/C	snv		0.24	2
rs7325927	FAM155A-IT1 ; FAM155A	0.925	0.040	13	107823165	intron variant	C/T	snv		0.38	2
rs3829382	FLT3	0.925	0.040	13	28003551	3 prime UTR variant	G/T	snv		0.46	2
rs11558961	GFAP	0.925	0.040	17	44907319	3 prime UTR variant	G/C;T	snv	0.27; 1.2E-05		2
rs759927375	H4C1 ; H3C1	0.925	0.040	6	26020589	missense variant	G/A;C	snv	1.2E-05; 8.0E-06		2
rs1161136341	HDAC9	0.925	0.080	7	18591621	missense variant	G/A	snv	8.0E-06	1.4E-05	2
rs774238794	HDAC9	0.925	0.080	7	18644690	missense variant	G/A;T	snv	4.1E-05; 4.1E-06		2
rs12230172	LOC105369844	0.882	0.040	12	75848895	intron variant	A/G	snv		0.48	2
rs3851634	POLR3B	0.882	0.040	12	106419124	intron variant	T/C	snv		0.22	2
rs8957	SLC2A4RG	0.925	0.040	20	63742354	missense variant	G/T	snv	0.71	0.78	2
rs648044	ZBTB16 ; LOC101928875	0.882	0.040	11	114160077	non coding transcript exon variant	A/G;T	snv			2
rs13332653		0.882	0.040	16	24578078	intergenic variant	T/G	snv		0.11	3
rs9933544		0.882	0.040	16	24576962	downstream gene variant	A/C	snv		0.29	3
rs6470745	CCDC26	0.882	0.040	8	129629675	intron variant	A/G	snv		0.18	3
rs891835	CCDC26	0.851	0.120	8	129479506	intron variant	T/G	snv		0.17	3