DisGeNET - a database of gene-disease associations

List of shared variants

Uric acid measurement (procedure), C0202239

Disease: Creatinine measurement, serum (procedure)

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
rs1260326	GCKR	0.645	0.600	2	27508073	missense variant	T/C;G	snv	0.63; 4.0E-06	0.68	81
rs1047891	CPS1	0.827	0.200	2	210675783	missense variant	C/A	snv	0.30	0.33	34
rs780093	GCKR	0.763	0.240	2	27519736	intron variant	T/C	snv		0.68	30
rs79105258	CUX2			12	111280427	intron variant	C/A;T	snv			24
rs9895661	BCAS3	0.882	0.200	17	61379228	non coding transcript exon variant	C/T	snv		0.69	10
rs10857147		1.000	0.040	4	80259918	intergenic variant	A/T	snv		0.25	9
rs17050272	LOC105373585	0.882	0.120	2	120548864	upstream gene variant	G/A	snv		0.33	9
rs62435145		1.000	0.040	7	1246931	regulatory region variant	G/T	snv		0.51	8
rs963837	LOC101928338 ; LINC02859	0.925	0.120	11	30727543	intergenic variant	T/C	snv		0.35	8
rs1106766	R3HDM2	0.882	0.120	12	57415673	intron variant	C/T	snv		0.19	7
rs1394125	UBE2Q2	0.882	0.200	15	75866642	intron variant	G/A;T	snv			7
rs3741414	INHBC	0.925	0.120	12	57450266	3 prime UTR variant	C/T	snv		0.19	7
rs3925584	LOC101928338	1.000	0.080	11	30738788	intergenic variant	T/C	snv		0.35	7
rs4014195		0.882	0.200	11	65739351	intergenic variant	C/G	snv		0.31	7
rs77924615	PDILT	1.000	0.080	16	20381010	intron variant	G/A	snv		0.16	7
rs729761	LOC105375069 ; LOC107986598	0.925	0.120	6	43836834	intron variant	T/A;G	snv			6
rs10109414		1.000	0.080	8	23893638	regulatory region variant	C/T	snv		0.37	5
rs10851885	NRG4	0.925	0.120	15	76012162	5 prime UTR variant	A/G	snv		0.18	5
rs10994856	A1CF	0.925	0.120	10	50885488	intron variant	G/A	snv		0.19	5
rs10994860	A1CF	0.925	0.120	10	50885664	5 prime UTR variant	C/T	snv		0.19	5
rs149454410	SLC2A9	0.925	0.120	4	9942000	missense variant	C/G;T	snv	4.0E-05; 3.2E-04		5
rs186459505	SFMBT1	0.925	0.120	3	52907083	missense variant	G/A;T	snv	1.1E-04; 4.0E-06		5
rs626277	DACH1	1.000	0.080	13	71773564	intron variant	A/C	snv		0.51	5
rs11554266	GNAS	1.000	0.040	20	58903791	splice region variant	C/G;T	snv	4.0E-06; 2.3E-03		4
rs138551969	VEGFA	1.000	0.040	6	43780749	missense variant	A/G	snv	1.2E-05	3.5E-05	4