DisGeNET - a database of gene-disease associations

List of associated variants

B-Cell Lymphomas, C0079731

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
rs1805087	MTR	0.496	0.800	1	236885200	missense variant	A/G	snv	0.20	0.21	135
rs387907272	MYD88	0.572	0.520	3	38141150	stop lost	T/C	snv	5.2E-05	7.0E-06	73
rs764643047	OGG1	0.851	0.120	3	9750336	missense variant	C/T	snv	4.0E-06		5
rs662	PON1	0.485	0.840	7	95308134	missense variant	T/C	snv	0.38	0.42	157
rs1472503583	PWWP3A	0.925	0.160	19	1360712	missense variant	C/T	snv	4.0E-06		4
rs78768932	PXN	0.882	0.080	12	120222977	missense variant	C/G;T	snv	5.4E-03	5.4E-03	6
rs149627368	REL			2	60922344	missense variant	T/C	snv	1.5E-04	1.0E-04	1
rs12144309	RSBN1			1	113772871	intron variant	C/T	snv		0.19	1
rs121912438	SOD1	0.605	0.520	21	31667299	missense variant	G/A;C;T	snv	1.2E-05; 8.0E-06		58
rs4880	SOD2	0.500	0.840	6	159692840	missense variant	A/G	snv	0.48	0.47	131
rs1799725	SOD2			6	159692840	missense variant	A/G	snv			1
rs1053023	STAT3	0.882	0.120	17	42313598	3 prime UTR variant	T/A;C	snv			4
rs1800629	TNF	0.472	0.920	6	31575254	upstream gene variant	G/A	snv	0.12	0.14	169
rs2230926	TNFAIP3	0.662	0.440	6	137874929	missense variant	T/C;G	snv	4.0E-06; 5.4E-02		27
rs1057520009	XPO1	0.790	0.200	2	61492337	missense variant	C/T	snv	4.4E-06		14
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