DisGeNET - a database of gene-disease associations

List of shared variants

Multiple Sclerosis, C0026769

Disease: Immune System Diseases

Source: GWASDB ×

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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
rs4648356	TTC34	1.000	0.080	1	2792599	intron variant	C/A	snv		0.39	3
rs11586238		0.925	0.160	1	116720516	regulatory region variant	C/G	snv		0.19	4
rs11676922	AFF3	0.925	0.160	2	100190478	intron variant	T/A	snv		0.51	4
rs13315591	FAM107A ; LOC107984079	0.925	0.160	3	58571114	intron variant	T/C	snv		0.15	4
rs212389	LOC105378083 ; LOC112267968	0.925	0.160	6	159068759	non coding transcript exon variant	G/A	snv		0.60	3
rs26232	MACIR	0.925	0.160	5	103261019	intron variant	C/T	snv		0.30	4
rs3093023	LOC105378122 ; CCR6	0.851	0.160	6	167120802	intron variant	G/A	snv		0.34	4
rs4750316	LINC02649 ; LINC02656	0.882	0.160	10	6351298	non coding transcript exon variant	C/G;T	snv			4
rs6859219	ANKRD55	0.925	0.160	5	56142753	intron variant	C/A	snv		0.20	4
rs874040		0.925	0.160	4	26106575	downstream gene variant	G/C	snv		0.29	4
rs934734	SPRED2	0.925	0.160	2	65368452	intron variant	G/A;T	snv		0.54	4
rs10903122		0.882	0.200	1	24977085	intergenic variant	A/G	snv		0.56	5
rs11712165	ARHGAP31	0.882	0.200	3	119399949	intron variant	T/G	snv		0.30	5
rs1250552	ZMIZ1	0.882	0.200	10	79298270	intron variant	A/C;G	snv			5
rs12928822	LOC105371082 ; RMI2	0.882	0.200	16	11310036	intron variant	C/T	snv		0.13	5
rs13003464	PUS10	0.827	0.200	2	60959694	intron variant	A/G	snv		0.50	7
rs13010713	LINC01934	0.882	0.200	2	181131318	intron variant	A/C;G	snv			5
rs13098911	CCR3	0.882	0.200	3	46193709	intron variant	C/G;T	snv			5
rs13151961	KIAA1109	0.827	0.200	4	122194347	intron variant	A/G	snv		0.11	5
rs13314993	LOC105377022	0.882	0.200	3	32973977	regulatory region variant	G/C;T	snv			5
rs17035378	PLEK ; LOC101927723	0.882	0.200	2	68371823	intron variant	T/A;C	snv			5
rs2816316	LOC105371664	0.882	0.200	1	192567683	intron variant	C/A	snv		0.79	5
rs296547	MROH3P	0.882	0.200	1	200923009	intron variant	T/C	snv		0.53	5
rs3748816	MMEL1	0.827	0.200	1	2595307	missense variant	A/G	snv	0.41	0.46	6
rs3761847	TRAF1	0.827	0.200	9	120927961	intron variant	G/A	snv		0.52	4