DisGeNET - a database of gene-disease associations

List of shared variants

Triglycerides measurement, C0202236

Disease: Uric acid measurement (procedure)

Source: GWASCAT ×

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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	55
rs780094	GCKR	0.658	0.400	2	27518370	intron variant	T/C	snv		0.67	35
rs780093	GCKR	0.763	0.240	2	27519736	intron variant	T/C	snv		0.68	16
rs11066280	HECTD4	0.742	0.280	12	112379979	intron variant	T/A	snv		7.0E-03	13
rs4149056	SLCO1B1	0.633	0.480	12	21178615	missense variant	T/C	snv	0.13	0.12	7
rs12423664	FBRSL1	1.000	0.040	12	132493308	intron variant	G/A	snv		0.10	6
rs17145738	TBL2	0.851	0.200	7	73568544	3 prime UTR variant	C/T	snv		0.11	5
rs3741414	INHBC	0.925	0.120	12	57450266	3 prime UTR variant	C/T	snv		0.19	5
rs79598313	KDF1			1	26958422	intron variant	C/A;T	snv			5
rs1178977	BAZ1B	0.925	0.120	7	73442719	splice region variant	A/G	snv	0.16	0.21	2