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
rs138729528	TP53	0.677	0.480	17	7675089	missense variant	G/A;C	snv	1.6E-05	25
rs28934574	TP53	0.658	0.440	17	7673776	missense variant	G/A;C	snv	4.0E-06	27
rs397516436	TP53	0.641	0.440	17	7674894	stop gained	G/A;C	snv		26
rs1057519738	MIR4728 ; ERBB2	0.790	0.160	17	39725079	missense variant	G/A	snv	4.0E-06	7
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
rs1057519919	MYCNOS ; MYCN	0.851	0.160	2	15942195	missense variant	C/T	snv		5
rs121913281	PIK3CA	0.623	0.520	3	179234296	missense variant	C/T	snv		37
rs121913413	CTNNB1	0.763	0.240	3	41224634	missense variant	C/A;T	snv		9
rs193920774	TP53	0.695	0.440	17	7673823	missense variant	C/A;T	snv		21
rs587781288	TP53	0.732	0.440	17	7675190	missense variant	C/A;T	snv		15
rs876660754	TP53	0.701	0.360	17	7675095	missense variant	C/A;T	snv		18
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
rs11540652	TP53	0.592	0.640	17	7674220	missense variant	C/A;G;T	snv	1.2E-05	42
rs121912657	TP53	0.683	0.480	17	7673806	missense variant	C/A;G;T	snv	4.0E-06	15
rs121913400	CTNNB1	0.683	0.360	3	41224610	missense variant	C/A;G;T	snv		17
rs28934576	TP53	0.554	0.600	17	7673802	missense variant	C/A;G;T	snv	4.0E-06; 1.6E-05	39
rs587778720	TP53	0.667	0.360	17	7674893	missense variant	C/A;G;T	snv	4.0E-06	25
rs587782329	TP53	0.677	0.280	17	7674217	missense variant	C/A;G;T	snv		16
rs587782664	TP53	0.742	0.320	17	7674252	missense variant	C/A;G;T	snv	4.0E-06	14
rs730882005	TP53	0.701	0.400	17	7674250	missense variant	C/A;G;T	snv	8.0E-06	20
rs730882008	TP53	0.683	0.440	17	7673775	missense variant	C/A;G;T	snv	4.0E-06	22