DisGeNET - a database of gene-disease associations

List of associated variants

Prostate carcinoma, C0600139

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	AF GENOME	Num. diseases
rs17036508	MTOR ; ANGPTL7	0.925	0.080	1	11195977	3 prime UTR variant	T/C	snv		9.0E-02	4
rs2297480	FDPS	0.851	0.280	1	155309691	non coding transcript exon variant	T/G	snv		0.28	4
rs3753793	CCN1 ; DDAH1	0.851	0.240	1	85580205	upstream gene variant	A/C	snv		0.26	4
rs11122573		1.000	0.080	1	230701434	upstream gene variant	C/T	snv		8.0E-02	3
rs12757998		0.925	0.080	1	182569343	downstream gene variant	C/T	snv		0.24	3
rs145889899	LDLRAD1	0.882	0.120	1	54010411	splice acceptor variant	C/T	snv	6.2E-04	2.4E-03	3
rs750392184	PIK3CD	0.882	0.160	1	9724850	missense variant	G/A	snv	4.0E-06		3
rs76826147	EPHB2	0.882	0.080	1	22913757	stop gained	A/G;T	snv	4.2E-06; 2.9E-03		3
rs10920531		0.925	0.080	1	202939708	downstream gene variant	A/C	snv		0.57	2
rs1131450	MTR	0.925	0.080	1	236898549	3 prime UTR variant	G/A	snv		0.28	2
rs1218582	KCNN3	0.925	0.080	1	154861707	intron variant	G/A	snv		0.46	2
rs12723593		0.925	0.080	1	182569447	downstream gene variant	C/G	snv		0.30	2
rs1350533716	PRDM2	0.925	0.080	1	13780080	missense variant	C/T	snv	4.0E-06	7.0E-06	2
rs143544690	RNASEL	0.925	0.080	1	182585927	missense variant	T/C	snv	3.5E-04	1.4E-03	2
rs2232853	CYB5R1	0.925	0.080	1	202962830	non coding transcript exon variant	G/A	snv		0.22	2
rs25655	CAPN2	0.925	0.080	1	223712706	missense variant	C/G	snv	1.00	0.99	2
rs2806864	PTGFRN	0.925	0.120	1	116927159	intron variant	C/G	snv		0.17	2
rs28372871	MTR	0.925	0.080	1	236795232	upstream gene variant	G/A;T	snv			2
rs3181082	CD1B	0.925	0.080	1	158332703	upstream gene variant	C/T	snv		0.11	2
rs35672330	EXO5	0.925	0.080	1	40514996	missense variant	T/C	snv	4.4E-02	4.4E-02	2
rs3806317	ANGPTL7 ; MTOR	0.925	0.080	1	11188159	intron variant	A/G	snv		3.4E-02	2
rs45609334	HSD3B1	0.925	0.080	1	119514623	missense variant	C/A	snv		0.76	2
rs561104	SELENOF	0.925	0.080	1	86906079	intron variant	C/T	snv		0.64	2
rs56250729	RNASEL	0.925	0.080	1	182586518	missense variant	T/C;G	snv	2.8E-05; 6.6E-03		2
rs636291	PEX14	0.925	0.080	1	10496040	intron variant	G/A	snv		0.55	2