DisGeNET - a database of gene-disease associations

List of shared variants

ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO, C1836232

Disease: Vitiligo

Source: ALL

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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
rs10484554	LOC112267902 ; HLA-B	0.807	0.200	6	31306778	intron variant	C/T	snv		0.12	11
rs12153855	TNXB	0.776	0.320	6	32107027	intron variant	T/C	snv		0.11	11
rs12198173	TNXB	0.827	0.240	6	32059031	intron variant	G/A	snv		0.10	9
rs13199524	TNXB	0.807	0.240	6	32098988	intron variant	C/T	snv		8.4E-02	9
rs3130473		0.882	0.160	6	31231431	intergenic variant	C/T	snv		0.23	6
rs34214527	TNXB	0.925	0.040	6	32046679	intron variant	C/T	snv		0.11	6
rs13211318		0.925	0.040	6	32134903	upstream gene variant	A/C	snv		0.11	5
rs2524123	HLA-B ; LINC02571 ; LOC112267902	0.925	0.040	6	31297537	intron variant	T/C	snv		0.34	5
rs3130424		0.925	0.040	6	31250462	intergenic variant	A/C;G;T	snv			5