DisGeNET - a database of gene-disease associations

Source: ALL

Variants associated to the Disease: Crohn Disease ×

Variants associated to the Gene: SLC22A5 ×

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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
rs1020856343	SLC22A5	0.851	0.240	5	132393705	missense variant	C/T	snv	4.0E-06		5
rs2631367	MIR3936HG ; SLC22A5	0.925	0.120	5	132369766	5 prime UTR variant	C/G	snv		0.59	4
rs2631372	SLC22A5 ; MIR3936HG	1.000	0.040	5	132367886	intron variant	G/C	snv		0.29	2