DisGeNET - a database of gene-disease associations

List of shared variants

Malignant neoplasm of pancreas, C0346647

Disease: Pancreatic carcinoma

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
rs1034925236	NR5A2	0.925	0.120	1	200048258	missense variant	G/C	snv			2
rs10500715	SBF2	0.925	0.120	11	9951515	intron variant	T/G	snv		0.39	2
rs10887710		0.925	0.120	10	80270029	downstream gene variant	T/C	snv		0.19	2
rs11085754	SMARCA4	0.925	0.120	19	11017920	intron variant	A/G	snv		0.41	2
rs11644043	BRD7	0.925	0.120	16	50327466	intron variant	T/C	snv		0.24	2
rs1235228469	PIK3CB	0.925	0.120	3	138684714	missense variant	C/A	snv	8.0E-06		2
rs12362504	SBF2 ; LOC101928008	0.925	0.120	11	9907995	intron variant	T/C	snv		0.37	2
rs12456874	LDLRAD4	0.925	0.120	18	13366863	intron variant	A/G	snv		0.20	2
rs1276300653	CAMK1 ; OGG1	0.925	0.120	3	9757072	missense variant	T/C	snv		7.0E-06	2
rs12939944	MAP2K4	0.925	0.120	17	12056502	intron variant	C/T	snv		0.45	2
rs1318	LOC101928045 ; PITPNC1	0.925	0.120	17	67695266	3 prime UTR variant	A/G	snv		0.30	2
rs13303010	KLHL17 ; NOC2L	0.925	0.120	1	959193	intron variant	G/A	snv	0.82	0.69	2
rs1336539869	CDK4	0.925	0.120	12	57751681	missense variant	C/G	snv			2
rs1339638227	CDKN2A	0.925	0.120	9	21971119	missense variant	T/C	snv	4.3E-06		2
rs138147246	OGG1	0.925	0.120	3	9756551	synonymous variant	A/G	snv	8.0E-06	1.4E-05	2
rs139632793	OGG1	0.925	0.120	3	9751114	missense variant	G/C	snv	5.2E-05	1.7E-04	2
rs141095230	MGMT	0.925	0.120	10	129536277	missense variant	C/A;T	snv	8.0E-06; 5.2E-05		2
rs1412335442	PIK3CG	0.925	0.120	7	106868317	missense variant	G/T	snv		7.0E-06	2
rs1448106115	PMS2	0.925	0.120	7	5989944	missense variant	T/C	snv	4.0E-06		2
rs145574072	OGG1	0.925	0.120	3	9754765	synonymous variant	T/C	snv	4.0E-06		2
rs145733073	UGT1A8 ; UGT1A9 ; UGT1A7 ; UGT1A10	0.925	0.120	2	233682175	missense variant	T/C;G	snv	4.0E-06; 1.4E-04		2
rs149243735	OGG1	0.925	0.120	3	9751076	missense variant	C/A	snv	4.0E-06		2
rs1547374	LOC105372815	0.925	0.120	21	42358786	downstream gene variant	A/G	snv		0.32	2
rs1552462		0.925	0.120	11	7235910	upstream gene variant	C/T	snv		2.7E-02	2
rs1630747	SLC5A3 ; MRPS6	0.925	0.120	21	34085692	intron variant	C/A	snv		0.69	2