DisGeNET - a database of gene-disease associations

List of associated variants

Malignant neoplasm of pancreas, C0346647

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
rs7106914	SBF2	1.000	0.120	11	9956424	intron variant	T/C	snv		0.38	1
rs10500715	SBF2	0.925	0.120	11	9951515	intron variant	T/G	snv		0.39	2
rs35385902	ADH1C ; ADH1B	0.807	0.240	4	99347122	missense variant	C/A;T	snv	2.0E-05; 1.1E-03		9
rs1693482	ADH1C ; ADH1B	0.807	0.240	4	99342808	missense variant	C/T	snv	0.34	0.31	12
rs698	ADH1C ; ADH1B	0.724	0.240	4	99339632	missense variant	T/A;C	snv	0.35		20
rs1229984	ADH1B	0.570	0.560	4	99318162	missense variant	T/C;G	snv	0.90		83
rs150495372	ADH1B	0.925	0.120	4	99313834	missense variant	C/T	snv	3.7E-04		3
rs12362504	SBF2 ; LOC101928008	0.925	0.120	11	9907995	intron variant	T/C	snv		0.37	2
rs1052133	OGG1 ; CAMK1	0.476	0.800	3	9757089	missense variant	C/G	snv	0.27	0.22	147
rs1276300653	CAMK1 ; OGG1	0.925	0.120	3	9757072	missense variant	T/C	snv		7.0E-06	2
rs138147246	OGG1	0.925	0.120	3	9756551	synonymous variant	A/G	snv	8.0E-06	1.4E-05	2
rs145574072	OGG1	0.925	0.120	3	9754765	synonymous variant	T/C	snv	4.0E-06		2
rs56053615	OGG1	0.851	0.120	3	9751845	missense variant	G/A;T	snv	3.4E-04; 4.0E-06		4
rs139632793	OGG1	0.925	0.120	3	9751114	missense variant	G/C	snv	5.2E-05	1.7E-04	2
rs149243735	OGG1	0.925	0.120	3	9751076	missense variant	C/A	snv	4.0E-06		2
rs13303010	KLHL17 ; NOC2L	0.925	0.120	1	959193	intron variant	G/A	snv	0.82	0.69	2
rs199976573	ABCG2	0.925	0.120	4	88132618	missense variant	C/T	snv	6.4E-05	5.6E-05	4
rs2075685	TMEM167A ; XRCC4	0.724	0.320	5	83076846	intron variant	G/A;T	snv			14
rs3751936	RPTOR	0.925	0.120	17	80964404	3 prime UTR variant	G/C	snv		0.20	2
rs62068300	RPTOR	0.925	0.120	17	80600927	intron variant	G/A;T	snv		5.7E-05	2
rs10887710		0.925	0.120	10	80270029	downstream gene variant	T/C	snv		0.19	2
rs1455311	LINC01088	0.925	0.160	4	79043433	intron variant	A/G	snv		0.14	2
rs11644322	WWOX	0.925	0.120	16	79005703	intron variant	C/T	snv		0.22	3
rs1801394	FASTKD3 ; MTRR	0.531	0.840	5	7870860	missense variant	A/G	snv	0.47	0.45	101
rs1051730	CHRNA3	0.641	0.600	15	78601997	synonymous variant	G/A	snv	0.27	0.26	43