DisGeNET - a database of gene-disease associations

Source: ALL

Variants associated to the Disease: Glioma ×

Variants associated to the Gene: CCDC26 ×

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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
rs55705857	CCDC26	0.732	0.080	8	129633446	intron variant	A/G	snv		3.9E-02	16
rs4295627	CCDC26	0.763	0.200	8	129673211	intron variant	T/G	snv		0.17	11
rs891835	CCDC26	0.851	0.120	8	129479506	intron variant	T/G	snv		0.17	5
rs10464870	CCDC26	0.882	0.040	8	129465577	intron variant	C/T	snv		0.80	3
rs6470745	CCDC26	0.882	0.040	8	129629675	intron variant	A/G	snv		0.18	3
rs12544799	CCDC26	1.000	0.040	8	129651264	intron variant	A/G	snv		0.34	1
rs16904140	CCDC26	1.000	0.040	8	129653397	intron variant	G/A	snv		0.19	1
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