DisGeNET - a database of gene-disease associations

List of associated variants

Malignant neoplasm of gallbladder, C0153452

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
rs2071011	CCKAR	1.000	0.080	4	26489811	intron variant	C/G;T	snv			1
rs3822222	CCKAR	1.000	0.080	4	26489030	intron variant	G/A	snv		0.14	1
rs915889	CCKAR	1.000	0.080	4	26484572	intron variant	G/A	snv		0.15	1
rs11082960	DCC	1.000	0.080	18	52999470	intron variant	G/T	snv		0.72	1
rs4077283	DCC	1.000	0.080	18	53019949	intron variant	G/A	snv		0.72	1
rs4078289	DCC	1.000	0.080	18	53020735	intron variant	A/G	snv		0.75	1
rs4940234	DCC	1.000	0.080	18	53012182	intron variant	C/A	snv		0.72	1
rs7233818	DCC	1.000	0.080	18	53009439	intron variant	T/A;C	snv			1
rs7504512	DCC	1.000	0.080	18	53003267	intron variant	G/A	snv		0.73	1
rs7504750	DCC	1.000	0.080	18	53021270	intron variant	C/A	snv		0.73	1
rs7506454	DCC	1.000	0.080	18	53007301	intron variant	G/A;T	snv			1
rs7506663	DCC	1.000	0.080	18	52993157	intron variant	T/A;C	snv			1
rs7507060	DCC	1.000	0.080	18	52999187	intron variant	C/T	snv		0.73	1
rs9304437	DCC	1.000	0.080	18	52995196	intron variant	T/G	snv		0.73	1
rs9944713	DCC	1.000	0.080	18	53008042	intron variant	C/A	snv		0.72	1
rs9957080	DCC	1.000	0.080	18	52994363	intron variant	G/T	snv		0.73	1
rs1800855	CCKAR	0.925	0.120	4	26489495	intron variant	A/G;T	snv	0.27		2
rs975334	CNTN4	0.925	0.080	3	2804632	intron variant	G/A	snv		0.50	2
rs4078288	DCC	0.882	0.120	18	53020881	intron variant	G/A	snv		0.73	3
rs7504990	DCC	0.851	0.120	18	52991406	intron variant	T/C	snv		0.73	4
rs4595552		0.790	0.080	11	125865825	intergenic variant	C/G;T	snv			7
rs1157	ALCAM	0.790	0.080	3	105576617	3 prime UTR variant	G/A	snv		0.16	7
rs13959	ALDH1A1	0.790	0.080	9	72930966	synonymous variant	G/A	snv	0.48	0.42	7
rs1169803481	EGFR	0.807	0.160	7	55198851	missense variant	A/G	snv	4.0E-06		7
rs1444424830	FASTK	0.790	0.080	7	151078923	missense variant	C/T	snv	4.6E-06	7.0E-06	7