DisGeNET - a database of gene-disease associations

List of associated variants

Hepatitis B, Chronic, C0524909

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
rs1010023	PNPLA3	0.851	0.080	22	43940218	intron variant	T/C	snv		0.20	4
rs1042522	TP53	0.426	0.800	17	7676154	missense variant	G/C;T	snv	0.67		242
rs1053004	STAT3	0.776	0.280	17	42314074	3 prime UTR variant	G/A	snv		0.48	11
rs1053005	STAT3	0.763	0.360	17	42313892	3 prime UTR variant	T/C	snv		0.25	10
rs1054690270	LOC101928953 ; GPT	0.827	0.160	8	144505907	frameshift variant	CT/-	delins			5
rs1131691014	TP53	0.439	0.800	17	7676154	frameshift variant	-/C	ins			214
rs11465817	IL23R	0.882	0.120	1	67255414	intron variant	C/A;T	snv			4
rs11556218	IL16	0.653	0.600	15	81305928	missense variant	T/G	snv	9.6E-02	0.12	27
rs117648444	IFNL4	0.882	0.160	19	39247938	missense variant	G/A	snv	0.25	8.1E-02	3
rs11977021		0.827	0.240	7	106288069	upstream gene variant	C/T	snv		0.22	5
rs12252	IFITM3	0.695	0.240	11	320772	splice region variant	A/G	snv	0.13	0.13	23
rs12354	LTBR	0.925	0.080	12	6390939	3 prime UTR variant	T/A;G	snv	1.6E-04; 0.76		2
rs12614	CYP21A2 ; CFB	0.851	0.160	6	31946402	missense variant	C/G;T	snv	4.1E-06; 0.12		5
rs12979860	IFNL4	0.547	0.520	19	39248147	intron variant	C/T	snv		0.39	84
rs12980275		0.701	0.360	19	39241143	upstream gene variant	A/G	snv		0.36	23
rs13419896	EPAS1	0.776	0.240	2	46329206	intron variant	G/A	snv		0.10	8
rs1353702185	MDM2	0.550	0.720	12	68839311	missense variant	C/G	snv	4.0E-06		79
rs1419881	TCF19	0.851	0.280	6	31162816	3 prime UTR variant	G/A	snv		0.50	4
rs148314165		0.925	0.160	6	137908902	intergenic variant	T/-	delins		2.0E-02	3
rs1799724	LTA ; TNF	0.600	0.680	6	31574705	upstream gene variant	C/T	snv		8.5E-02	47
rs1799945	LOC108783645 ; HFE	0.452	0.760	6	26090951	missense variant	C/G;T	snv	0.11	0.10	226
rs1800562	LOC108783645 ; HFE	0.435	0.880	6	26092913	missense variant	G/A	snv	3.3E-02	3.8E-02	262
rs1800610	TNF	0.807	0.320	6	31576050	intron variant	G/A	snv		8.4E-02	7
rs1800629	TNF	0.472	0.920	6	31575254	upstream gene variant	G/A	snv	0.12	0.14	169
rs1800630	TNF ; LOC100287329 ; LTA	0.701	0.480	6	31574699	upstream gene variant	C/A	snv		0.14	17