DisGeNET - a database of gene-disease associations

List of shared variants

Multiple Sclerosis, C0026769

Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO

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
rs2523535		0.851	0.200	6	31368473	intron variant	A/G	snv		0.32	7
rs2736172	PRRC2A ; SNORA38	0.882	0.160	6	31623121	non coding transcript exon variant	C/T	snv	0.41	0.29	6
rs6906846	HLA-B ; USP8P1	0.851	0.280	6	31277959	non coding transcript exon variant	A/G	snv		0.67	6
rs9391858	TSBP1-AS1 ; TSBP1	0.925	0.080	6	32373621	intron variant	A/G	snv		0.13	6
rs3094609	HCG27	0.925	0.080	6	31197789	non coding transcript exon variant	T/C	snv	0.86	0.89	5
rs3130558	PSORS1C1	0.925	0.080	6	31129406	intron variant	C/G	snv		0.77	5
rs3130975	C6orf15 ; PSORS1C1	0.925	0.080	6	31114061	upstream gene variant	C/T	snv		0.27	5
rs3130981	CDSN ; PSORS1C1	0.925	0.080	6	31116036	missense variant	T/C;G	snv	0.76		5
rs3131009	PSORS1C1	0.925	0.080	6	31131055	intron variant	G/A;C	snv			5
rs528878831	PSORS1C1	0.925	0.080	6	31131055	intron variant	G/A;C	snv			5
rs7382297	HLA-B	0.925	0.080	6	31279290	intron variant	T/C;G	snv			5