DisGeNET - a database of gene-disease associations

List of associated variants

Lymphoma, Non-Hodgkin, C0024305

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
rs1346044	WRN	0.708	0.440	8	31167138	missense variant	T/C	snv	0.24	0.23	23
rs1353759920	TP73	0.851	0.120	1	3707593	missense variant	C/A	snv		2.1E-05	4
rs13706	CDC6	0.776	0.200	17	40300899	missense variant	G/A;C	snv	0.15; 8.0E-06		11
rs1401417	CRY2	0.882	0.160	11	45858559	intron variant	C/G	snv		0.19	3
rs1447708158	RAF1	1.000	0.120	3	12604160	synonymous variant	C/T	snv		7.0E-06	1
rs144848	BRCA2	0.653	0.440	13	32332592	missense variant	A/C	snv	0.28	0.23	29
rs1448674651	TYMS ; ENOSF1	0.667	0.560	18	671384	missense variant	G/A;C	snv	4.0E-06		23
rs146713238	LOC105379176 ; IL4	1.000	0.120	5	132679861	missense variant	G/A	snv	3.2E-05	8.4E-05	1
rs147603016	FGFR4	0.925	0.160	5	177093286	synonymous variant	G/A;C	snv	1.5E-04; 8.2E-06		3
rs148701087	SHMT1 ; MIR6778	1.000	0.120	17	18340762	missense variant	G/A	snv	6.4E-04	8.8E-04	1
rs1494555	IL7R	0.790	0.120	5	35871088	missense variant	G/A	snv	0.64	0.72	8
rs150865017	ALDH1L1	1.000	0.120	3	126154627	missense variant	G/A;T	snv	1.6E-05; 4.0E-06		1
rs161870	MTRR	0.925	0.160	5	7878079	synonymous variant	T/C	snv	0.18	0.21	2
rs16917496	KMT5A	0.689	0.360	12	123409283	3 prime UTR variant	C/G;T	snv			21
rs16941	BRCA1	0.827	0.240	17	43092418	missense variant	T/C;G	snv	0.35		7
rs1695	GSTP1	0.457	0.880	11	67585218	missense variant	A/G	snv	0.34	0.36	188
rs16994592	CD70	1.000	0.120	19	6586487	intron variant	T/C	snv		9.4E-02	1
rs17024869	NPAS2	0.708	0.320	2	100843581	intron variant	T/C	snv		8.3E-02	18
rs17655	BIVM-ERCC5 ; ERCC5	0.597	0.560	13	102875652	missense variant	G/C	snv	0.28	0.30	52
rs17723799	MIR143 ; CARMN	1.000	0.120	5	149427514	non coding transcript exon variant	C/T	snv		9.9E-02	1
rs1785882	CARD16 ; LOC107984381	1.000	0.120	11	105052348	intron variant	A/T	snv		0.45	1
rs1790192	CXCR5	1.000	0.120	11	118886482	non coding transcript exon variant	G/A;C	snv	0.58		1
rs1799782	XRCC1	0.474	0.800	19	43553422	missense variant	G/A	snv	9.5E-02	7.0E-02	151
rs1799793	ERCC2	0.557	0.640	19	45364001	missense variant	C/A;T	snv	7.1E-06; 0.29		72
rs1799931	NAT2	0.742	0.320	8	18400860	missense variant	G/A	snv	5.8E-02	3.9E-02	14