DisGeNET - a database of gene-disease associations

List of shared variants

Triglycerides measurement, C0202236

Disease: Arthritis, Gouty

Source: GWASDB ×

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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
rs12539316		0.925	0.120	7	73563568	downstream gene variant	A/G	snv		0.28	5
rs1260333		0.882	0.160	2	27525757	downstream gene variant	A/G	snv		0.58	8
rs780090	GCKR ; FNDC4	0.925	0.120	2	27495607	upstream gene variant	T/C;G	snv			4
rs4665963	TRIM54	0.925	0.120	2	27305824	splice region variant	T/C	snv	0.35	0.43	3
rs1051921	MLXIPL	0.925	0.120	7	73593613	3 prime UTR variant	G/A	snv		0.15	6
rs1178979	BAZ1B	0.925	0.120	7	73442100	3 prime UTR variant	T/C	snv		0.21	6
rs13232120	TBL2	0.925	0.120	7	73568980	3 prime UTR variant	A/T	snv		0.11	6
rs13472	ZNF513 ; SNX17	0.925	0.120	2	27377372	3 prime UTR variant	G/A	snv		0.38	3
rs17145738	TBL2	0.851	0.200	7	73568544	3 prime UTR variant	C/T	snv		0.11	6
rs2240466	BAZ1B	0.925	0.120	7	73441939	3 prime UTR variant	G/A	snv		9.2E-02	4
rs1049817	GTF3C2	0.925	0.120	2	27328100	synonymous variant	A/G	snv	0.42	0.48	3
rs1528533	SNX17	0.925	0.120	2	27372889	non coding transcript exon variant	G/C	snv		0.47	3
rs2074755	BAZ1B	0.807	0.240	7	73462836	non coding transcript exon variant	T/C	snv		9.2E-02	4
rs2286276	TBL2	0.925	0.120	7	73573024	non coding transcript exon variant	C/T	snv		0.28	5
rs1260326	GCKR	0.645	0.600	2	27508073	missense variant	T/C;G	snv	0.63; 4.0E-06	0.68	25
rs1919127	C2orf16	0.925	0.120	2	27578626	missense variant	T/C	snv	0.31	0.27	6
rs1919128	C2orf16	0.882	0.120	2	27578892	missense variant	A/G	snv	0.30	0.24	6
rs3749147	GPN1 ; CCDC121	0.882	0.120	2	27629051	missense variant	G/A	snv	0.23	0.20	6
rs799166		0.925	0.120	7	73637602	intergenic variant	C/G	snv		0.16	4
rs11613352	R3HDM2	0.827	0.160	12	57398797	intron variant	C/T	snv		0.19	5
rs11681351	GCKR	0.925	0.120	2	27520556	intron variant	G/A	snv		0.36	3
rs11974409	TBL2	0.925	0.120	7	73575060	intron variant	A/G	snv		0.16	6
rs12056034	BAZ1B	0.882	0.160	7	73464315	intron variant	A/G	snv		9.2E-02	4
rs13022873	ZNF512	0.882	0.120	2	27592643	intron variant	A/C;T	snv			6
rs13030345	MRPL33	0.925	0.120	2	27780307	intron variant	G/T	snv		0.15	3