DisGeNET - a database of gene-disease associations

Source: ALL

Variants associated to the Disease: Protein measurement ×

Variants associated to the Gene: SOCS4 ×

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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
rs11851178	SOCS4			14	55035411	intron variant	A/G	snv		0.44	1
rs1187873	SOCS4			14	55033533	intron variant	T/C	snv		0.26	1
rs1187874	SOCS4			14	55031385	intron variant	A/G	snv		0.74	1
rs1212641	SOCS4			14	55029413	intron variant	G/A;C	snv			1
rs17128132	SOCS4			14	55040039	intron variant	C/T	snv		0.40	1
rs17128136	SOCS4			14	55043392	synonymous variant	G/A;T	snv	7.3E-02		1
rs1952085	SOCS4			14	55045555	3 prime UTR variant	C/A;G	snv			1
rs1952438	SOCS4			14	55031230	intron variant	G/A	snv		0.15	1
rs7149965	SOCS4			14	55041473	intron variant	G/A;C;T	snv			1
rs7150145	SOCS4			14	55041542	intron variant	G/A	snv		0.41	1
rs8008134	SOCS4			14	55040802	intron variant	T/C	snv		0.52	1
rs1187878	SOCS4 ; WDHD1			14	55026632	intron variant	T/C	snv		0.59	1
rs1209087	SOCS4 ; WDHD1			14	55026502	intron variant	C/G;T	snv			1
rs1201378	WDHD1 ; SOCS4			14	55026690	intron variant	T/A;C	snv	0.57		1