DisGeNET - a database of gene-disease associations

List of shared variants

Malignant neoplasm of ovary, C1140680

Disease: ovarian neoplasm

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
rs10088218	LINC00824	0.851	0.120	8	128531703	intron variant	G/A	snv		0.13	4
rs10098821	LINC00824	0.882	0.120	8	128546982	intron variant	C/T	snv		7.6E-02	3
rs11084033	LOC105372441	0.882	0.120	19	50850699	intron variant	C/A;T	snv			4
rs1136905	HLA-DRB3 ; HLA-DRB5	0.882	0.120	6	32518660	missense variant	T/A;C	snv	4.2E-03		3
rs11683487	NMI	0.882	0.120	2	151286035	intron variant	G/T	snv		0.36	3
rs11782652	CHMP4C	0.851	0.120	8	81741409	intron variant	A/G	snv		6.6E-02	4
rs13063604	RUVBL1	0.882	0.120	3	128085887	intron variant	G/A	snv		0.23	3
rs137852691	OPCML	0.925	0.120	11	132657203	missense variant	G/A;C	snv	8.0E-06		2
rs1444192401	KRT7	0.882	0.120	12	52235347	missense variant	G/A	snv			4
rs1456079929	PGR	0.851	0.120	11	101042001	missense variant	C/A	snv	8.0E-06		5
rs147961867	MAPK3	0.882	0.120	16	30121998	missense variant	T/C	snv	5.6E-05	2.8E-05	3
rs1516982	LINC00824	0.882	0.120	8	128521400	intron variant	A/G	snv		0.16	3
rs1805129	CHEK2	0.882	0.120	22	28734470	synonymous variant	T/C	snv	3.6E-02	4.0E-02	3
rs185229225	BOD1L1	0.851	0.120	4	13607505	intron variant	T/C	snv			4
rs186724	AHCYL1	0.882	0.120	1	110018293	intron variant	C/G;T	snv			3
rs2072590	HAGLR ; HAGLROS	0.851	0.120	2	176177905	non coding transcript exon variant	A/C;T	snv			4
rs2191249	BRIP1	0.882	0.120	17	61758503	intron variant	T/G	snv		0.79	3
rs2228026	TEP1	0.882	0.120	14	20395890	synonymous variant	A/G	snv	4.7E-02	3.8E-02	3
rs2287497	WRAP53 ; TP53	0.882	0.120	17	7689462	intron variant	G/A	snv		0.25	3
rs2287498	WRAP53 ; TP53	0.882	0.120	17	7689242	synonymous variant	C/T	snv	0.13	0.14	4
rs266851	KLK15 ; LOC105372441	0.882	0.120	19	50833083	intron variant	C/T	snv		0.20	3
rs2708861	HUS1	0.851	0.120	7	47977120	intron variant	T/G	snv		0.46	6
rs28933370	MIR4728 ; ERBB2	0.882	0.120	17	39725125	missense variant	A/G	snv		7.0E-06	3
rs34289250	BRIP1	0.925	0.120	17	61803285	intron variant	T/C	snv		7.8E-03	2
rs34529039	CEBPA ; CEBPA-DT	0.882	0.120	19	33301725	synonymous variant	C/A	snv	0.19	0.16	3