DisGeNET - a database of gene-disease associations

List of shared variants

Mammary Neoplasms, C1458155

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
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
rs587777790	PIK3CA	0.732	0.280	3	179199690	missense variant	G/A	snv		12
rs104886003	PIK3CA	0.562	0.440	3	179218303	missense variant	G/A;C	snv	4.0E-06	34
rs121913274	PIK3CA	0.645	0.320	3	179218304	missense variant	A/C;G;T	snv		28
rs121913275	PIK3CA	0.672	0.320	3	179218305	missense variant	G/A;C;T	snv	4.0E-06	25
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
rs121913283	PIK3CA	0.724	0.440	3	179234286	missense variant	G/A;T	snv	4.0E-06	14
rs121913281	PIK3CA	0.623	0.520	3	179234296	missense variant	C/T	snv		37
rs121913279	PIK3CA	0.526	0.560	3	179234297	missense variant	A/G;T	snv	4.0E-06; 4.0E-06	45
rs1057519932	PIK3CA	0.683	0.320	3	179234298	missense variant	T/G	snv		22
rs1057519738	MIR4728 ; ERBB2	0.790	0.160	17	39725079	missense variant	G/A	snv	4.0E-06	7
rs80338963	SMAD4	0.776	0.280	18	51065548	missense variant	C/A;G;T	snv		11
rs377767347	SMAD4	0.742	0.520	18	51065549	missense variant	G/A;C;T	snv		13
rs121913233	HRAS ; LRRC56	0.627	0.520	11	533874	missense variant	T/A;C;G	snv		20
rs28933406	LRRC56 ; HRAS	0.667	0.480	11	533875	missense variant	G/C;T	snv		17
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
rs104894230	HRAS ; LRRC56	0.564	0.600	11	534288	missense variant	C/A;G;T	snv		36
rs104894229	LRRC56 ; HRAS	0.564	0.600	11	534289	missense variant	C/A;G;T	snv		52
rs11554273	GNAS	0.689	0.240	20	58909365	missense variant	C/A;G;T	snv	4.0E-06	17
rs121913495	GNAS	0.672	0.400	20	58909366	missense variant	G/A;T	snv		15
rs1057519960	SF3B2	0.827	0.280	11	66063413	missense variant	A/G	snv		7
rs1057519912	MED12	0.776	0.200	X	71129408	missense variant	C/G;T	snv		5