DisGeNET - a database of gene-disease associations

List of shared variants

Kidney Failure, Chronic, C0022661

Disease: Chronic kidney disease stage 5

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
rs10137082	IL25	0.925	0.080	14	23370824	upstream gene variant	C/T	snv		0.23	2
rs10404257	ACTN4	0.925	0.080	19	38645846	upstream gene variant	G/A	snv		0.50	2
rs10808565	PVT1	0.925	0.080	8	127995166	non coding transcript exon variant	C/T	snv		0.31	2
rs11089781	APOL3	0.925	0.080	22	36160720	stop gained	G/A	snv	1.6E-02	6.5E-02	2
rs115489112	NPHS1	0.925	0.080	19	35830918	missense variant	G/A	snv	4.3E-04	1.6E-03	2
rs12137135		0.925	0.080	1	22348728	intergenic variant	A/C;G	snv			2
rs12431381	RTN1	0.925	0.080	14	59643053	intron variant	T/C	snv		0.35	2
rs12437854	LOC107983974	0.925	0.080	15	93598604	intron variant	T/G	snv		0.10	2
rs12917114		0.925	0.080	15	47852953	intron variant	C/T	snv		8.9E-02	2
rs145640112	KLKB1	0.925	0.080	4	186250267	missense variant	A/C;G	snv	1.8E-04; 4.0E-06		2
rs146400394	NPHS1	0.925	0.080	19	35842486	missense variant	C/T	snv	6.8E-05	4.9E-05	2
rs1516792	IL1A	0.925	0.080	2	112778356	intron variant	G/A	snv			2
rs16347	IL1A	0.925	0.080	2	112774138	3 prime UTR variant	-/TGAA	delins		0.70	2
rs17709344	LOC107983974	0.925	0.080	15	93608310	intron variant	G/A	snv		4.0E-02	2
rs183962941	UMOD	0.925	0.080	16	20343125	intron variant	G/A	snv		1.1E-02	2
rs2391335	EFNB2	0.925	0.080	13	106519637	non coding transcript exon variant	T/C;G	snv		0.50	2
rs2413396	MYH9	0.925	0.080	22	36312039	intron variant	C/G;T	snv	0.88		2
rs2802723	SDCCAG8	0.925	0.080	1	243335010	intron variant	T/C;G	snv			2
rs281874682	COL4A5	0.925	0.080	X	108598805	missense variant	C/A;T	snv	5.5E-06		2
rs2838302	SIK1	0.925	0.080	21	43419273	intron variant	A/G	snv	1.0E-01		2
rs301640	LINC01442	0.925	0.080	13	60885853	intron variant	C/G;T	snv			2
rs370819889	ALB	0.925	0.080	4	73416353	missense variant	C/A;T	snv	8.0E-06; 9.6E-05		2
rs373971520	GNG7	0.925	0.080	19	2568808	intron variant	CA/-;CACA	delins			2
rs374118649	FLNB	0.925	0.080	3	58097965	missense variant	A/G;T	snv	3.6E-05		2
rs4253373	KLKB1	0.925	0.080	4	186250250	missense variant	C/A	snv	6.7E-04	2.5E-03	2