DisGeNET - a database of gene-disease associations

List of shared variants

Malignant Uterine Corpus Neoplasm, C0153574

Disease: Adenocarcinoma of pancreas

Source: CLINVAR ×

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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
rs104886003	PIK3CA	0.562	0.440	3	179218303	missense variant	G/A;C	snv	4.0E-06	34
rs104894226	LRRC56 ; HRAS	0.658	0.560	11	534285	missense variant	C/A;G;T	snv		23
rs104894228	LRRC56 ; HRAS	0.605	0.560	11	534286	missense variant	C/A;G;T	snv		30
rs104894229	LRRC56 ; HRAS	0.564	0.600	11	534289	missense variant	C/A;G;T	snv		52
rs104894230	HRAS ; LRRC56	0.564	0.600	11	534288	missense variant	C/A;G;T	snv		36
rs1057519738	MIR4728 ; ERBB2	0.790	0.160	17	39725079	missense variant	G/A	snv	4.0E-06	7
rs1057519747	TP53	0.716	0.280	17	7675094	missense variant	A/C;G;T	snv		17
rs1057519886	CTNNB1	0.752	0.240	3	41224609	missense variant	T/A;C;G	snv		11
rs1057519919	MYCNOS ; MYCN	0.851	0.160	2	15942195	missense variant	C/T	snv		5
rs1057519932	PIK3CA	0.683	0.320	3	179234298	missense variant	T/G	snv		22
rs1057519936	PIK3CA	0.776	0.200	3	179234284	missense variant	A/G;T	snv		11
rs1057519937	PIK3CA	0.776	0.200	3	179234285	missense variant	T/C	snv		11
rs1057519943	POLE	0.790	0.160	12	132676598	missense variant	G/C;T	snv		5
rs1057519944	POLE	0.882	0.160	12	132676599	missense variant	G/A	snv		5
rs1057519977	TP53	0.763	0.360	17	7675189	missense variant	G/C	snv		13
rs1057519978	TP53	0.763	0.360	17	7675191	missense variant	A/C;G;T	snv		12
rs1057519981	TP53	0.689	0.440	17	7674251	missense variant	A/C;G;T	snv		20
rs1057519991	TP53	0.662	0.440	17	7675076	missense variant	T/A;C;G	snv	4.0E-06	19
rs1057520002	TP53	0.695	0.360	17	7674242	missense variant	A/C;G	snv		20
rs1057520007	TP53	0.701	0.440	17	7674917	missense variant	T/A;C;G	snv		17
rs11540652	TP53	0.592	0.640	17	7674220	missense variant	C/A;G;T	snv	1.2E-05	42
rs121912651	TP53	0.605	0.680	17	7674221	missense variant	G/A;C	snv	4.0E-06	37
rs121912657	TP53	0.683	0.480	17	7673806	missense variant	C/A;G;T	snv	4.0E-06	15
rs121912666	TP53	0.645	0.360	17	7674872	missense variant	T/C;G	snv	8.0E-06	24
rs121913233	HRAS ; LRRC56	0.627	0.520	11	533874	missense variant	T/A;C;G	snv		20