DisGeNET - a database of gene-disease associations

List of associated variants

Kidney Failure, Acute, C0022660

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
rs12457893	BCL2	1.000	0.080	18	63258928	intron variant	A/C	snv		0.39	1
rs41507953	EPHX2	0.790	0.280	8	27500988	missense variant	A/G	snv	8.7E-02	0.13	10
rs10854554		0.925	0.080	22	19623159	regulatory region variant	A/G	snv		0.18	2
rs775020499	LRSAM1	1.000	0.080	9	127467764	missense variant	A/G	snv	8.2E-06		1
rs8094315	BCL2	1.000	0.080	18	63268814	intron variant	A/G	snv		0.17	1
rs9617814		1.000	0.080	22	19622420	regulatory region variant	A/G	snv		0.22	1
rs1444669684	CDKN2B-AS1 ; CDKN2A	0.658	0.480	9	21994285	missense variant	C/A;T	snv			36
rs1370328347	CSH1	1.000	0.080	17	63895621	missense variant	C/A;T	snv	1.0E-05; 1.0E-05		1
rs1800471	TGFB1	0.597	0.840	19	41352971	missense variant	C/G;T	snv	5.6E-02		48
rs767816037	CSH2	1.000	0.080	17	63872725	missense variant	C/G;T	snv	4.5E-05		1
rs696	NFKBIA	0.708	0.520	14	35401887	3 prime UTR variant	C/T	snv		0.45	22
rs782818582	ADAMTS13	0.882	0.160	9	133456116	stop gained	C/T	snv	1.2E-05	7.0E-06	3
rs561633150	SLC2A9	0.925	0.200	4	9980627	missense variant	C/T	snv	6.1E-04	9.1E-05	2
rs62341639		0.925	0.080	4	184238281	intergenic variant	C/T	snv		0.20	2
rs2233417	NFKBIA	1.000	0.080	14	35402888	intron variant	C/T	snv	0.14	0.13	1
rs4680	COMT ; MIR4761	0.442	0.920	22	19963748	missense variant	G/A	snv	0.46	0.44	249
rs1800629	TNF	0.472	0.920	6	31575254	upstream gene variant	G/A	snv	0.12	0.14	169
rs1800777	CETP	0.724	0.280	16	56983407	missense variant	G/A	snv	3.7E-02	2.8E-02	17
rs2233406	NFKBIA	0.732	0.440	14	35405593	upstream gene variant	G/A	snv		0.26	12
rs2276415	AQP11 ; CLNS1A	0.882	0.160	11	77590296	missense variant	G/A	snv	0.14	0.13	6
rs121907896	SLC22A12	0.851	0.200	11	64591825	missense variant	G/A	snv	1.8E-04	8.4E-05	5
rs1451506414	SLC22A12	0.882	0.200	11	64598561	synonymous variant	G/A	snv			4
rs1050851	NFKBIA	1.000	0.080	14	35403720	synonymous variant	G/A	snv	0.17	0.15	1
rs1955656	SERPINA5	1.000	0.080	14	94579038	intron variant	G/A	snv		0.14	1
rs2093266	SERPINA5 ; SERPINA4	1.000	0.080	14	94566450	intron variant	G/A	snv		0.15	1