DisGeNET - a database of gene-disease associations

Source: GWASDB

Variants associated to the Disease: Uric acid measurement (procedure) ×

Variants associated to the Gene: SLC16A9 ×

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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
rs12356193	SLC16A9	0.925	0.120	10	59653595	intron variant	A/G	snv		0.12	3
rs1171614	SLC16A9	0.882	0.200	10	59709780	5 prime UTR variant	T/C	snv		0.79	2
rs1171616	SLC16A9	0.882	0.200	10	59708831	intron variant	G/T	snv		0.79	2
rs1171617	SLC16A9	0.925	0.120	10	59707424	intron variant	G/A;T	snv			2
rs1171659	SLC16A9	0.925	0.120	10	59684606	intron variant	A/G	snv		0.31	2