DisGeNET - a database of gene-disease associations

List of associated variants

Epithelial ovarian cancer, C0677886

Source: GWASCAT ×

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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
rs74917072	UBE2F ; UBE2F-SCLY	0.882	0.120	2	238022053	intron variant	G/A;T	snv			1
rs7651446	TIPARP	0.882	0.120	3	156689208	intron variant	G/T	snv		7.9E-02	2
rs10260419	THSD7A	0.882	0.120	7	11524758	intron variant	C/G	snv		0.26	1
rs10069690	TERT	0.595	0.560	5	1279675	intron variant	C/T	snv		0.36	16
rs17329882	SYNPO2	0.925	0.120	4	119028805	intron variant	A/C;T	snv			1
rs11175194	SRGAP1	0.925	0.120	12	63871057	intron variant	G/A	snv		0.15	1
rs9303542	SKAP1	0.882	0.120	17	48334138	intron variant	A/G	snv		0.34	2
rs12039431	RSPO1	1.000	0.120	1	37616450	intron variant	G/A	snv	0.24	0.21	1
rs662	PON1	0.485	0.840	7	95308134	missense variant	T/C	snv	0.38	0.42	1
rs17130142	PKN2-AS1	1.000	0.120	1	87773925	intron variant	G/A	snv		6.5E-02	1
rs1243180	MLLT10	0.790	0.160	10	21626690	intron variant	T/A	snv		0.23	2
rs183211	LRRC37A2 ; NSF	0.882	0.160	17	46710944	intron variant	G/A	snv	0.28	0.30	3
rs1800562	LOC108783645 ; HFE	0.435	0.880	6	26092913	missense variant	G/A	snv	3.3E-02	3.8E-02	18
rs4525119	LOC107984198 ; AKR1C3	0.925	0.120	10	5049762	intron variant	C/T	snv		0.30	1
rs192876988	LOC105377300	0.851	0.120	4	79376097	intergenic variant	T/C	snv		1.6E-02	1
rs3820282	LOC105376845 ; WNT4	0.925	0.120	1	22141722	intron variant	C/T	snv		0.13	1
rs56318008	LOC105376845 ; WNT4	0.925	0.120	1	22143914	5 prime UTR variant	C/T	snv		0.13	1
rs7643459	LOC101927394 ; LMCD1-AS1	0.925	0.120	3	7963141	intron variant	G/C;T	snv			1
rs10088218	LINC00824	0.851	0.120	8	128531703	intron variant	G/A	snv		0.13	2
rs314276	LIN28B	0.807	0.280	6	104960124	intron variant	A/C	snv		0.65	2
rs13181	KLC3 ; ERCC2	0.487	0.760	19	45351661	stop gained	T/A;G	snv	4.0E-06; 0.32		1
rs17401966	KIF1B	0.790	0.280	1	10325413	intron variant	A/G	snv		0.24	1
rs1834481	IL18	0.882	0.160	11	112153104	non coding transcript exon variant	C/G	snv		0.16	1
rs5498	ICAM4 ; ICAM1	0.531	0.760	19	10285007	missense variant	A/G	snv	0.44	0.37	2
rs11651755	HNF1B	0.763	0.160	17	37739849	intron variant	T/C	snv		0.52	4