DisGeNET - a database of gene-disease associations

Source: GWASCAT

Variants associated to the Disease: Arthritis, Psoriatic ×

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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
rs458017	MFSD4B ; REV3L	0.925	0.080	6	111374888	missense variant	T/C	snv	5.9E-02	5.6E-02	2
rs4683946		0.925	0.080	3	101896982	intron variant	G/T	snv		0.19	2
rs114212579	SKIV2L ; CYP21A2	1.000	0.080	6	31968280	non coding transcript exon variant	G/T	snv			1
rs114265779	TRIM26	1.000	0.080	6	30213844	upstream gene variant	C/T	snv			1
rs114383947	MUC22	1.000	0.080	6	31010940	intron variant	C/T	snv			1
rs114598684	MICA	1.000	0.080	6	31413173	intron variant	C/T	snv			1
rs114757170	MRPS18B ; PPP1R10	1.000	0.080	6	30618254	intron variant	G/A	snv			1
rs115112280	HCG23 ; TSBP1-AS1	1.000	0.080	6	32390772	non coding transcript exon variant	T/A;G	snv			1
rs115145466		1.000	0.080	6	32251264	upstream gene variant	C/A;T	snv			1
rs115429782	HLA-B ; LINC02571 ; LOC112267902	1.000	0.080	6	31297975	intron variant	T/C	snv			1
rs115429849	MICC	1.000	0.080	6	30416827	intron variant	G/A	snv			1
rs115529844	LOC105375010	1.000	0.080	6	29850244	non coding transcript exon variant	C/T	snv			1
rs115618145	TRIM31	1.000	0.080	6	30102498	upstream gene variant	C/G	snv			1
rs115645848	GABBR1	1.000	0.080	6	29622938	intron variant	C/G;T	snv			1
rs115872194	BAG6	1.000	0.080	6	31639897	intron variant	C/A;T	snv			1
rs115928623	HLA-A ; MICD	1.000	0.080	6	29971371	intron variant	A/T	snv			1
rs116199901	HCG18 ; HCG17	1.000	0.080	6	30315875	intron variant	G/C	snv			1
rs116340302	RPL15P4 ; MCCD1	1.000	0.080	6	31528604	non coding transcript exon variant	A/T	snv			1
rs116805908	POU5F1 ; PSORS1C3	1.000	0.080	6	31173746	non coding transcript exon variant	C/T	snv			1
rs12044149	C1orf141	0.925	0.080	1	67135003	intron variant	G/C;T	snv			1
rs12356475	CTNNA3	1.000	0.080	10	66001962	intron variant	T/C	snv		0.15	1
rs13190932	TRAF3IP2 ; TRAF3IP2-AS1	1.000	0.080	6	111591867	missense variant	G/A	snv	5.3E-02	5.0E-02	1
rs13191343	HLA-C ; HLA-B	1.000	0.080	6	31273332	intron variant	C/G;T	snv		0.13	1
rs145699582	INSL6	1.000	0.080	9	5169600	intron variant	C/T	snv		2.5E-03	1
rs149997688	DDR1	1.000	0.080	6	30893833	intron variant	G/A	snv			1