DisGeNET - a database of gene-disease associations

Source: ALL

Variants associated to the Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO ×

Variants associated to the Gene: TNXB ×

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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
rs12153855	TNXB	0.776	0.320	6	32107027	intron variant	T/C	snv		0.11	11
rs185819	TNXB	0.851	0.200	6	32082290	missense variant	T/A;C;G	snv	8.2E-06; 0.58; 4.1E-06		10
rs2269426	TNXB	0.807	0.280	6	32108722	intron variant	G/A	snv		0.35	10
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
rs8283	ATF6B ; TNXB	0.882	0.120	6	32115523	3 prime UTR variant	A/G	snv		0.25	7
rs34214527	TNXB	0.925	0.040	6	32046679	intron variant	C/T	snv		0.11	6
rs429150	TNXB	1.000		6	32107786	intron variant	T/C;G	snv			6
rs12211410	TNXB	0.925	0.120	6	32081646	missense variant	C/G;T	snv	5.6E-05; 7.7E-02; 3.7E-05		5
rs2856448	TNXB	1.000		6	32046798	intron variant	A/G	snv		0.52	4
rs28732175	TNXB ; ATF6B	1.000		6	32117501	intron variant	C/T	snv		2.4E-02	4