DisGeNET - a database of gene-disease associations

List of associated variants

Acquired Immunodeficiency Syndrome, C0001175

Source: ALL

Results per page

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
rs2844511		0.807	0.200	6	31422007	intron variant	A/G;T	snv			10
rs2395029	HCP5	0.790	0.320	6	31464003	non coding transcript exon variant	T/G	snv	2.7E-02	2.4E-02	12
rs2284178	HCP5	0.925	0.120	6	31464348	non coding transcript exon variant	C/T	snv		0.44	6
rs2248462		0.807	0.240	6	31479019	downstream gene variant	G/A	snv		0.19	10
rs2516509	MICB-DT	0.882	0.160	6	31482217	intron variant	T/C	snv		0.19	7
rs909253	LTA ; LOC100287329	0.641	0.600	6	31572536	intron variant	A/G;T	snv			34
rs1800629	TNF	0.472	0.920	6	31575254	upstream gene variant	G/A	snv	0.12	0.14	169
rs3093662	TNF	0.851	0.200	6	31576412	intron variant	A/G	snv		7.1E-02	9
rs9368699	SNHG32 ; SNORD48	0.851	0.200	6	31834764	non coding transcript exon variant	T/C	snv		3.2E-02	8
rs12198173	TNXB	0.827	0.240	6	32059031	intron variant	G/A	snv		0.10	9
rs241447	TAP2	0.827	0.280	6	32828974	missense variant	T/C	snv	0.31	0.26	11
rs3732378	CX3CR1	0.620	0.720	3	39265671	missense variant	G/A	snv	0.14	0.12	48
rs3732379	CX3CR1	0.637	0.680	3	39265765	missense variant	C/T	snv	0.22	0.22	38
rs1799864	CCR2	0.572	0.680	3	46357717	missense variant	G/A	snv	0.13	0.12	68
rs1020608562	CCR5AS ; CCR5	0.807	0.160	3	46373738	missense variant	T/C	snv	4.0E-06		9
rs1369619997	KIDINS220			2	8731746	missense variant	G/C	snv	4.0E-06		1
rs374596032	KIDINS220			2	8813255	missense variant	A/C;G	snv	4.0E-06; 8.0E-06		1