DisGeNET - a database of gene-disease associations

List of associated variants

Autoantibody measurement, C1272321

Source: GWASDB ×

Results per page

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
rs7528684	FCRL3	0.752	0.560	1	157701026	upstream gene variant	A/G	snv		0.57	1
rs1990760	IFIH1	0.672	0.480	2	162267541	missense variant	C/T	snv	0.50	0.45	4
rs1004446	IGF2 ; INS-IGF2 ; IGF2-AS	0.827	0.240	11	2148913	intron variant	G/A	snv		0.37	3
rs2069762	IL2	0.672	0.560	4	122456825	upstream gene variant	A/C	snv		0.24	1
rs4788084	IL27	0.827	0.200	16	28528527	downstream gene variant	C/T	snv		0.36	3
rs12722495	IL2RA	0.851	0.200	10	6055320	intron variant	T/C	snv		7.0E-02	1
rs689	INS ; INS-IGF2	0.776	0.280	11	2160994	splice region variant	A/T	snv	0.73	0.60	1
rs12518099	LINC01339	0.925	0.120	5	90250292	intron variant	A/G;T	snv			3
rs1701704	LOC105369781 ; IKZF4	0.851	0.200	12	56018703	intron variant	T/G	snv		0.25	5
rs7171171	LOC107984725	0.925	0.120	15	38614840	intergenic variant	A/G	snv		0.24	1
rs6859	NECTIN2	0.827	0.120	19	44878777	3 prime UTR variant	A/G	snv		0.58	6
rs12610605	NECTIN2	1.000	0.080	19	44867581	intron variant	G/A	snv		0.15	2
rs1871047	NECTIN2	1.000	0.080	19	44848489	intron variant	A/G	snv		0.31	2
rs377702	NECTIN2	1.000	0.080	19	44859410	intron variant	G/A	snv		0.34	2
rs1048699	PPP1R37 ; MARK4	1.000	0.080	19	45147128	3 prime UTR variant	C/T	snv		9.0E-02	2
rs1114832	PPP1R37 ; MARK4	1.000	0.080	19	45132943	intron variant	C/T	snv		9.2E-02	2
rs3184504	SH2B3 ; ATXN2	0.572	0.600	12	111446804	missense variant	T/A;C;G	snv	0.67		24
rs13266634	SLC30A8 ; LOC105375716	0.724	0.480	8	117172544	missense variant	C/A;T	snv	0.29		3
rs7903146	TCF7L2	0.554	0.680	10	112998590	intron variant	C/G;T	snv			8
rs2075650	TOMM40	0.662	0.360	19	44892362	intron variant	A/G	snv	0.13	0.13	20
rs157580	TOMM40	0.882	0.160	19	44892009	intron variant	G/A	snv		0.69	11
rs8106922	TOMM40	1.000	0.080	19	44898409	intron variant	A/G	snv		0.36	4
rs2304256	TYK2	0.732	0.360	19	10364976	missense variant	C/A	snv	0.27	0.23	3
rs3788013	UBASH3A	0.851	0.240	21	42421219	intron variant	C/A	snv		0.44	1
rs4689388	WFS1	0.882	0.360	4	6268329	upstream gene variant	G/A	snv		0.64	3