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	Num. diseases
rs1034925236	NR5A2	0.925	0.120	1	200048258	missense variant	G/C	snv		2
rs1037189404	MUC1	0.776	0.280	1	155187519	missense variant	C/T	snv		8
rs1042522	TP53	0.426	0.800	17	7676154	missense variant	G/C;T	snv	0.67	242
rs1045485	CASP8	0.637	0.480	2	201284866	missense variant	G/A;C;T	snv	4.0E-06; 9.0E-02	34
rs104894094	CDKN2A	0.763	0.200	9	21971058	missense variant	C/A;G;T	snv	8.5E-06; 4.3E-06	12
rs104894230	HRAS ; LRRC56	0.564	0.600	11	534288	missense variant	C/A;G;T	snv		73
rs1057519921	NFE2L2	0.763	0.240	2	177234231	missense variant	T/C	snv		10
rs111033565	PRSS1	0.742	0.120	7	142751938	missense variant	G/A	snv	1.2E-05	11
rs111966833	SPINK1	0.776	0.320	5	147828053	missense variant	G/A;C	snv	4.5E-03	8
rs1130409	APEX1	0.555	0.720	14	20456995	missense variant	T/A;C;G	snv	4.0E-06; 4.0E-06; 0.42	72
rs1131691014	TP53	0.439	0.800	17	7676154	frameshift variant	-/C	ins		214
rs1131691021	TP53	0.716	0.120	17	7675097	missense variant	A/C;G	snv		21
rs11571836	BRCA2	0.827	0.200	13	32399302	3 prime UTR variant	A/G;T	snv		6
rs1194611372	S100A11	0.763	0.320	1	152032679	missense variant	A/C	snv		9
rs1209809979	AKR1A1	0.925	0.120	1	45568989	missense variant	A/G	snv	4.0E-06	3
rs121434592	AKT1	0.595	0.640	14	104780214	missense variant	C/T	snv	4.0E-06	54
rs121912651	TP53	0.605	0.680	17	7674221	missense variant	G/A;C	snv	4.0E-06	53
rs121912666	TP53	0.645	0.360	17	7674872	missense variant	T/C;G	snv	8.0E-06	34
rs121913343	TP53	0.611	0.520	17	7673803	missense variant	G/A;C;T	snv	1.2E-05	44
rs121913527	KRAS	0.807	0.320	12	25225628	missense variant	C/A;G;T	snv		9
rs121913529	KRAS	0.492	0.680	12	25245350	missense variant	C/A;G;T	snv	4.0E-06	144
rs121913530	KRAS	0.583	0.640	12	25245351	missense variant	C/A;G;T	snv		63
rs1229984	ADH1B	0.570	0.560	4	99318162	missense variant	T/C;G	snv	0.90	83
rs1235228469	PIK3CB	0.925	0.120	3	138684714	missense variant	C/A	snv	8.0E-06	2
rs1273593548	PIK3CG	0.716	0.160	7	106867593	missense variant	T/G	snv	8.4E-06	19