DisGeNET - a database of gene-disease associations

Source: ALL

Variants associated to the Gene: ADARB2 ×

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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
rs2820651	ADARB2	1.000	0.040	10	1429570	intron variant	C/A	snv		0.14	2
rs11250741	ADARB2	1.000	0.040	10	1697382	intron variant	T/C;G	snv		2.9E-02	1
rs11814309	ADARB2	1.000	0.040	10	1702876	intron variant	T/A	snv		0.12	1
rs12245785	ADARB2	1.000	0.040	10	1696668	intron variant	T/C	snv		3.7E-02	1
rs150155092	ADARB2			10	1727688	intron variant	TA/-;TATA	delins		7.0E-06	1
rs1874984	ADARB2			10	1689677	intron variant	G/C	snv		0.43	1
rs1909436	ADARB2	1.000	0.040	10	1697417	intron variant	C/T	snv		0.23	1
rs2892394	ADARB2	1.000	0.040	10	1698084	intron variant	C/A;T	snv			1
rs6560743	ADARB2			10	1594941	intron variant	T/C	snv		0.75	1
rs7087342	ADARB2	1.000		10	1613599	intron variant	G/A	snv		0.11	1
rs7896371	ADARB2			10	1686832	intron variant	C/T	snv		0.41	1
rs7924155	ADARB2	1.000	0.040	10	1694438	intron variant	T/G	snv		0.15	1
rs138734198	ADARB2 ; LINC00200	1.000	0.080	10	1217099	missense variant	C/T	snv	1.8E-04	7.0E-04	1
rs145022376	ADARB2 ; LINC00200	1.000	0.120	10	1186289	intron variant	C/-	delins		9.1E-03	1
rs4939821	CTIF ; LOC105372105	1.000	0.040	18	48845622	intron variant	C/T	snv		0.24	1
rs80356518	FLNB ; FLNB-AS1	1.000	0.080	3	58163161	stop gained	T/C;G	snv	4.0E-06		1
rs8640	FLNB ; FLNB-AS1			3	58168600	synonymous variant	C/T	snv	0.39	0.37	1