DisGeNET - a database of gene-disease associations

List of associated variants

Epithelial ovarian cancer, C0677886

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
rs2070074	GALT	0.742	0.360	9	34649445	missense variant	A/G	snv	9.2E-02	7.4E-02	12
rs17702471	GPC6	0.925	0.120	13	93224864	upstream gene variant	A/G	snv		0.16	2
rs115344852	GPX6	1.000	0.120	6	28518321	intron variant	A/C	snv			1
rs2190503	GRB10	0.925	0.120	7	50674920	intron variant	A/G;T	snv			2
rs768623239	GSTM1 ; GSTM2	0.662	0.640	1	109689278	missense variant	A/G	snv	1.5E-05		26
rs1695	GSTP1	0.457	0.880	11	67585218	missense variant	A/G	snv	0.34	0.36	188
rs2072590	HAGLR ; HAGLROS	0.851	0.120	2	176177905	non coding transcript exon variant	A/C;T	snv			4
rs11651755	HNF1B	0.763	0.160	17	37739849	intron variant	T/C	snv		0.52	9
rs7405776	HNF1B	0.807	0.120	17	37733029	intron variant	G/A;C	snv			6
rs757210	HNF1B	0.807	0.160	17	37736525	intron variant	C/G;T	snv			6
rs4759314	HOTAIR	0.649	0.440	12	53968051	non coding transcript exon variant	G/A	snv		0.93	31
rs7958904	HOTAIR	0.724	0.200	12	53963768	non coding transcript exon variant	C/A;G	snv			15
rs17427875	HOXA11 ; HOXA11-AS	0.925	0.120	7	27185939	non coding transcript exon variant	A/T	snv		0.15	2
rs5498	ICAM4 ; ICAM1	0.531	0.760	19	10285007	missense variant	A/G	snv	0.44	0.37	99
rs1834481	IL18	0.882	0.160	11	112153104	non coding transcript exon variant	C/G	snv		0.16	5
rs3783553	IL1A	0.667	0.480	2	112774138	3 prime UTR variant	-/TGAA	delins			26
rs2252673	INSR	0.882	0.120	19	7150407	intron variant	C/G	snv		0.75	3
rs3745546	INSR	0.925	0.120	19	7211805	intron variant	G/A;C	snv			2
rs17401966	KIF1B	0.790	0.280	1	10325413	intron variant	A/G	snv		0.24	7
rs1002076	KIF1B	0.925	0.120	1	10378834	3 prime UTR variant	G/A	snv		0.33	2
rs13181	KLC3 ; ERCC2	0.487	0.760	19	45351661	stop gained	T/A;G	snv	4.0E-06; 0.32		134
rs16917496	KMT5A	0.689	0.360	12	123409283	3 prime UTR variant	C/G;T	snv			21
rs61764370	KRAS	0.662	0.320	12	25207290	3 prime UTR variant	A/C	snv		6.2E-02	29
rs314276	LIN28B	0.807	0.280	6	104960124	intron variant	A/C	snv		0.65	10
rs10088218	LINC00824	0.851	0.120	8	128531703	intron variant	G/A	snv		0.13	4