DisGeNET - a database of gene-disease associations

List of shared variants

Uric acid measurement (procedure), C0202239

Disease: Arthritis, Gouty

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
rs671	ALDH2	0.529	0.840	12	111803962	missense variant	G/A	snv	1.9E-02	5.8E-03	116
rs1260326	GCKR	0.645	0.600	2	27508073	missense variant	T/C;G	snv	0.63; 4.0E-06	0.68	81
rs780094	GCKR	0.658	0.400	2	27518370	intron variant	T/C	snv		0.67	62
rs2231142	ABCG2	0.583	0.680	4	88131171	missense variant	G/C;T	snv	4.0E-06; 0.12		56
rs653178	ATXN2	0.672	0.600	12	111569952	intron variant	C/T	snv		0.67	41
rs780093	GCKR	0.763	0.240	2	27519736	intron variant	T/C	snv		0.68	30
rs4072037	MUC1	0.732	0.240	1	155192276	splice acceptor variant	C/A;T	snv	0.59		22
rs10774625	ATXN2	0.763	0.320	12	111472415	intron variant	A/G	snv		0.66	13
rs1260333		0.882	0.160	2	27525757	downstream gene variant	A/G	snv		0.58	12
rs17145738	TBL2	0.851	0.200	7	73568544	3 prime UTR variant	C/T	snv		0.11	11
rs9895661	BCAS3	0.882	0.200	17	61379228	non coding transcript exon variant	C/T	snv		0.69	10
rs17050272	LOC105373585	0.882	0.120	2	120548864	upstream gene variant	G/A	snv		0.33	9
rs17145750	MLXIPL	0.925	0.120	7	73612048	intron variant	C/A;T	snv			9
rs2079742	BCAS3	0.851	0.240	17	61388336	non coding transcript exon variant	T/C	snv		0.20	9
rs2244608	HNF1A ; HNF1A-AS1	0.882	0.160	12	120979185	intron variant	A/G	snv		0.29	9
rs1051921	MLXIPL	0.925	0.120	7	73593613	3 prime UTR variant	G/A	snv		0.15	8
rs11099098		0.925	0.120	4	80248758	intergenic variant	G/C;T	snv			8
rs1106766	R3HDM2	0.882	0.120	12	57415673	intron variant	C/T	snv		0.19	7
rs1171614	SLC16A9	0.882	0.200	10	59709780	5 prime UTR variant	T/C	snv		0.79	7
rs1178977	BAZ1B	0.925	0.120	7	73442719	splice region variant	A/G	snv	0.16	0.21	7
rs1394125	UBE2Q2	0.882	0.200	15	75866642	intron variant	G/A;T	snv			7
rs16890979	SLC2A9	0.827	0.200	4	9920543	missense variant	C/T	snv	0.24	0.29	7
rs3741414	INHBC	0.925	0.120	12	57450266	3 prime UTR variant	C/T	snv		0.19	7
rs4014195		0.882	0.200	11	65739351	intergenic variant	C/G	snv		0.31	7
rs6449213	SLC2A9 ; LOC105374476	0.827	0.240	4	9992591	intron variant	C/T	snv		0.82	7