DisGeNET - a database of gene-disease associations

List of associated variants

Hepatitis, C0019158

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
rs17879702	HLA-DRB1	1.000	0.080	6	32584346	missense variant	G/A	snv	3.2E-02	5.7E-02	2
rs2237061	CXCL14	1.000	0.080	5	135576640	intron variant	C/T	snv		8.4E-02	2
rs1047782	TDP2			6	24650503	3 prime UTR variant	T/C;G	snv			1
rs10484389	CASC15			6	22075033	intron variant	C/T	snv		6.0E-02	1
rs11025185	NAV2			11	19572259	intron variant	G/A	snv		2.4E-03	1
rs1432133	GABRG3			15	26983199	intron variant	A/G;T	snv			1
rs17568725				5	171743637	TF binding site variant	C/A	snv		0.19	1
rs2174866	LOC107983981			15	53172023	intergenic variant	A/T	snv		6.2E-02	1
rs3087943	TDP2			6	24650533	3 prime UTR variant	A/G	snv		0.18	1
rs4467099	LOC400499			16	11449038	missense variant	C/A;T	snv	0.66		1
rs4683336	KRBOX1 ; ACKR2			3	42818461	intron variant	C/T	snv		0.61	1
rs7518687	LOC105371604			1	168663745	intergenic variant	A/T	snv		0.22	1
rs8014067	SYT16			14	62086539	intron variant	A/T	snv		0.79	1
rs9522267				13	111544020	intergenic variant	G/A	snv		0.32	1
rs368234815	IFNL4	0.742	0.280	19	39248514	frameshift variant	TT/G;T	delins			15
rs878854066	TP53	0.439	0.800	17	7676153	missense variant	GG/AC	mnv			213
rs1131691014	TP53	0.439	0.800	17	7676154	frameshift variant	-/C	ins			214