DisGeNET - a database of gene-disease associations

List of shared variants

Glioblastoma, C0017636

Disease: Glioblastoma Multiforme

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
rs11548193	BCAT2	0.925	0.040	19	48799813	missense variant	G/A;C	snv	0.14		2
rs11558961	GFAP	0.925	0.040	17	44907319	3 prime UTR variant	G/C;T	snv	0.27; 1.2E-05		2
rs11670188	BTBD2	0.925	0.040	19	2014038	non coding transcript exon variant	A/G	snv		0.16	2
rs1558650888	DNMT3A	0.925	0.040	2	25234308	missense variant	G/A	snv			2
rs2291427	ALOX5	0.925	0.040	10	45440776	intron variant	A/G;T	snv			2
rs3829382	FLT3	0.925	0.040	13	28003551	3 prime UTR variant	G/T	snv		0.46	2
rs7325927	FAM155A-IT1 ; FAM155A	0.925	0.040	13	107823165	intron variant	C/T	snv		0.38	2
rs759927375	H4C1 ; H3C1	0.925	0.040	6	26020589	missense variant	G/A;C	snv	1.2E-05; 8.0E-06		2
rs7732320	SSBP2	0.925	0.040	5	81423306	intron variant	C/T	snv		0.22	2
rs8957	SLC2A4RG	0.925	0.040	20	63742354	missense variant	G/T	snv	0.71	0.78	2
rs9642393	EGFR	0.925	0.040	7	55177954	intron variant	T/C	snv		0.24	2
rs10464870	CCDC26	0.882	0.040	8	129465577	intron variant	C/T	snv		0.80	3
rs1249080185	EPHB2	0.882	0.080	1	22784698	missense variant	G/A	snv			3
rs12645561	NEIL3	0.882	0.120	4	177339718	intron variant	C/A;T	snv			3
rs13332653		0.882	0.040	16	24578078	intergenic variant	T/G	snv		0.11	3
rs1346787	EFEMP1 ; LOC112268416	0.882	0.040	2	55865477	downstream gene variant	C/A;G;T	snv			3
rs145929329	CDKN2B-AS1	0.882	0.040	9	22066213	intron variant	TTTT/-;T;TT;TTT;TTTTT;TTTTTT;TTTTTTTTTT	delins		0.58	3
rs2033214	RBBP6	0.882	0.040	16	24566199	intron variant	T/G	snv		0.14	3
rs6470745	CCDC26	0.882	0.040	8	129629675	intron variant	A/G	snv		0.18	3
rs879254044	MSH2	0.925	0.040	2	47475148	missense variant	G/A;C;T	snv			3
rs9933544		0.882	0.040	16	24576962	downstream gene variant	A/C	snv		0.29	3
rs1029044314	DDR1	0.851	0.040	6	30898095	missense variant	G/A	snv			4
rs10852606	HEATR3	0.882	0.040	16	50094961	intron variant	T/A;C	snv			4
rs11233250	MIR4300HG	0.882	0.040	11	82685972	intron variant	C/T	snv		0.11	4
rs12230172	LOC105369844	0.882	0.040	12	75848895	intron variant	A/G	snv		0.48	4