DisGeNET - a database of gene-disease associations

List of shared variants

Corpuscular Hemoglobin Concentration Mean, C4528257

Disease: Gout

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
rs3184504	SH2B3 ; ATXN2	0.572	0.600	12	111446804	missense variant	T/A;C;G	snv	0.67		92
rs653178	ATXN2	0.672	0.600	12	111569952	intron variant	C/T	snv		0.67	41
rs11065987		0.807	0.280	12	111634620	intergenic variant	A/G	snv		0.29	17
rs10774625	ATXN2	0.763	0.320	12	111472415	intron variant	A/G	snv		0.66	13
rs9472135	LOC107986598	0.925	0.120	6	43842065	intron variant	T/A;C;G	snv			9
rs4766578	ATXN2	0.851	0.200	12	111466567	intron variant	T/A	snv		0.66	8
rs881858	LOC105375069 ; LOC107986598	0.882	0.200	6	43838872	intron variant	G/A;C	snv			7
rs10480300	PRKAG2	0.925	0.120	7	151708919	intron variant	C/T	snv		0.24	6
rs12216125		0.925	0.120	6	25997230	intron variant	C/T	snv		0.26	6
rs2032447	H3C3 ; H2BC3 ; H2AC5P	0.925	0.120	6	26044141	non coding transcript exon variant	A/G	snv	4.1E-06; 0.67	0.67	6
rs2071303	LOC108783645 ; HFE	0.882	0.120	6	26091108	splice region variant	T/C	snv	0.38	0.36	6
rs3887266	SLC17A3	0.925	0.120	6	25843518	intron variant	C/T	snv		8.9E-02	6
rs4886755	NRG4	0.925	0.120	15	76005791	non coding transcript exon variant	A/G;T	snv	0.49		6
rs729761	LOC105375069 ; LOC107986598	0.925	0.120	6	43836834	intron variant	T/A;G	snv			6
rs7753826		0.925	0.120	6	26042011	upstream gene variant	T/A;C	snv			6
rs7756117	H3C3	0.882	0.160	6	26046337	upstream gene variant	G/A	snv		0.69	6
rs9472138	LOC107986598	0.882	0.160	6	43844025	downstream gene variant	C/T	snv		0.24	6
rs11072566	NRG4	0.925	0.120	15	76001630	intron variant	A/G	snv		0.45	5
rs1150660		0.925	0.120	6	26101212	upstream gene variant	A/C	snv		0.73	5
rs115810	TRIM38	0.925	0.120	6	25975655	intron variant	G/A;C	snv			5
rs1165196	SLC17A1	0.882	0.200	6	25812922	missense variant	G/A	snv	0.62	0.66	5
rs1165215	SLC17A1	0.882	0.200	6	25798704	3 prime UTR variant	G/A	snv		0.66	5
rs129129	TRIM38	0.925	0.120	6	25960801	upstream gene variant	A/G	snv		0.73	5
rs13197601	SLC17A1	0.882	0.200	6	25785707	intron variant	G/A	snv		0.32	5