DisGeNET - a database of gene-disease associations

List of associated variants

Adenocarcinoma of prostate, C0007112

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	AF GENOME	Num. diseases
rs121913365	BRAF	0.776	0.320	7	140753332	missense variant	T/A;G	snv			8
rs121913409	CTNNB1	0.708	0.400	3	41224646	missense variant	C/A;G;T	snv			9
rs121913413	CTNNB1	0.763	0.240	3	41224634	missense variant	C/A;T	snv			9
rs1800562	LOC108783645 ; HFE	0.435	0.880	6	26092913	missense variant	G/A	snv	3.3E-02	3.8E-02	9
rs869025608	MAP2K1	0.763	0.400	15	66435117	missense variant	G/C;T	snv			9
rs1057519947	PPP2R1A	0.790	0.160	19	52212730	missense variant	G/A	snv			9
rs397507484	BRAF	0.752	0.480	7	140753333	missense variant	T/A;C;G	snv			10
rs121913407	CTNNB1	0.763	0.240	3	41224645	missense variant	T/C;G	snv			10
rs121913412	CTNNB1	0.724	0.280	3	41224633	missense variant	A/C;G;T	snv			10
rs1057519938	PIK3CA	0.776	0.160	3	179203764	missense variant	A/C;T	snv			10
rs1057519939	PIK3CA	0.776	0.160	3	179203763	missense variant	A/C	snv			10
rs121913284	PIK3CA	0.776	0.160	3	179203765	missense variant	T/A;G	snv			10
rs121913357	BRAF	0.742	0.320	7	140781603	stop gained	C/A;G;T	snv			11
rs1057519883	CDKN2A	0.742	0.280	9	21971120	missense variant	C/G;T	snv			11
rs1057519886	CTNNB1	0.752	0.240	3	41224609	missense variant	T/A;C;G	snv			11
rs121913228	CTNNB1	0.742	0.200	3	41224621	missense variant	T/C;G	snv			11
rs121913396	CTNNB1	0.732	0.200	3	41224607	missense variant	A/C;G;T	snv			11
rs121913496	LRRC56 ; HRAS	0.724	0.440	11	533873	missense variant	C/A;G;T	snv			11
rs121913272	PIK3CA	0.752	0.400	3	179210192	missense variant	T/C;G	snv			11
rs121913287	PIK3CA	0.752	0.400	3	179199088	missense variant	G/A	snv			11
rs1057520005	TP53	0.742	0.360	17	7673800	missense variant	C/A;G	snv			11
rs587777790	PIK3CA	0.732	0.280	3	179199690	missense variant	G/A	snv			12
rs1057519978	TP53	0.763	0.360	17	7675191	missense variant	A/C;G;T	snv			12
rs1057519999	TP53	0.763	0.160	17	7674247	missense variant	T/C;G	snv			12
rs1057520006	TP53	0.752	0.240	17	7673799	missense variant	A/C;G;T	snv			12