DisGeNET - a database of gene-disease associations

List of shared variants

Hepatocarcinogenesis, C1512409

Disease: Hepatitis B

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
rs1800562	LOC108783645 ; HFE	0.435	0.880	6	26092913	missense variant	G/A	snv	3.3E-02	3.8E-02	262
rs671	ALDH2	0.529	0.840	12	111803962	missense variant	G/A	snv	1.9E-02	5.8E-03	116
rs738409	PNPLA3	0.557	0.720	22	43928847	missense variant	C/G	snv	0.28	0.22	88
rs12979860	IFNL4	0.547	0.520	19	39248147	intron variant	C/T	snv		0.39	84
rs28934571	TP53	0.645	0.360	17	7674216	missense variant	C/A;G	snv			31
rs11134527	MIR218-2 ; SLIT3	0.677	0.400	5	168768351	intron variant	G/A	snv		0.25	24
rs2596542	MICA-AS1 ; MICA	0.724	0.200	6	31398818	upstream gene variant	C/T	snv		0.41	18
rs1049606	CCND2-AS1 ; CCND2	0.851	0.160	12	4273870	5 prime UTR variant	C/T	snv		0.58	4
rs246871	ITK ; MED7	0.882	0.160	5	157158243	intron variant	T/C	snv		0.42	3
rs6710479	LOC105373977 ; PDCD1	0.882	0.200	2	241855866	intron variant	T/C	snv		0.51	3
rs1367492395	TP53	0.925	0.160	17	7673589	missense variant	G/T	snv			2