DisGeNET - a database of gene-disease associations

List of associated variants

B-Cell Lymphomas, C0079731

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
rs2509049	H2AX	0.827	0.160	11	119095811	upstream gene variant	C/A;T	snv			6
rs9610	IL10RA ; SMIM35	0.882	0.240	11	118001371	3 prime UTR variant	G/A;T	snv	0.51		4
rs604714	DPAGT1	0.925	0.120	11	119099986	intron variant	C/A	snv		0.31	3
rs3218674	ATM	1.000	0.120	11	108244860	synonymous variant	C/G;T	snv	1.1E-02	1.1E-02	2
rs78768932	PXN	0.882	0.080	12	120222977	missense variant	C/G;T	snv	5.4E-03	5.4E-03	6
rs141185042	DNM1L			12	32707409	missense variant	A/T	snv	4.1E-06	7.0E-06	1
rs17655	BIVM-ERCC5 ; ERCC5	0.597	0.560	13	102875652	missense variant	G/C	snv	0.28	0.30	52
rs539846	BMF	1.000	0.120	15	40105735	intron variant	G/C;T	snv			2
rs1053023	STAT3	0.882	0.120	17	42313598	3 prime UTR variant	T/A;C	snv			4
rs2227945	BRCA1	1.000	0.080	17	43092113	missense variant	T/C;G	snv	2.5E-03	1.0E-02	2
rs1800477	BCL2	0.763	0.480	18	63318540	missense variant	C/T	snv	1.8E-02	4.9E-03	12
rs17757541	BCL2	0.827	0.240	18	63212453	intron variant	C/G;T	snv			7
rs25487	XRCC1	0.441	0.800	19	43551574	missense variant	T/C	snv	0.68	0.71	205
rs1799782	XRCC1	0.474	0.800	19	43553422	missense variant	G/A	snv	9.5E-02	7.0E-02	151
rs1472503583	PWWP3A	0.925	0.160	19	1360712	missense variant	C/T	snv	4.0E-06		4
rs121912438	SOD1	0.605	0.520	21	31667299	missense variant	G/A;C;T	snv	1.2E-05; 8.0E-06		58
rs9808753	IFNGR2	0.701	0.400	21	33415005	missense variant	A/G	snv	0.20	0.18	17