DisGeNET - a database of gene-disease associations

List of associated variants

Precursor Cell Lymphoblastic Leukemia Lymphoma, C1961102

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
rs121913448	ABL1	0.827	0.120	9	130862976	missense variant	G/A	snv			5
rs1057519773	ABL1	0.851	0.160	9	130872901	missense variant	T/A;C;G	snv			4
rs121913451	ABL1	0.851	0.160	9	130872903	missense variant	C/A;G	snv			4
rs112141546	ADAMTS18	1.000	0.120	16	77367618	missense variant	C/A;G;T	snv	4.0E-06; 1.4E-03		1
rs1966862	ARHGAP24	0.790	0.120	4	85766908	intron variant	A/G	snv		0.14	8
rs10821936	ARID5B	0.742	0.200	10	61963818	intron variant	C/T	snv		0.69	11
rs7089424	ARID5B	0.752	0.200	10	61992400	intron variant	T/G	snv		0.32	10
rs10740055	ARID5B	0.790	0.240	10	61958720	intron variant	C/A	snv		0.49	7
rs10994982	ARID5B	0.790	0.120	10	61950345	intron variant	A/G	snv		0.49	7
rs6479778	ARID5B	0.827	0.200	10	61929318	intron variant	T/C;G	snv			5
rs7073837	ARID5B	0.851	0.120	10	61940136	intron variant	A/C	snv	0.58	0.64	4
rs10821938	ARID5B	0.925	0.120	10	61965014	intron variant	A/C	snv		0.56	2
rs7896246	ARID5B	0.925	0.120	10	61964631	intron variant	A/G	snv		0.74	2
rs4245595	ARID5B	1.000	0.120	10	61963136	intron variant	C/T	snv		0.69	1
rs7087125	ARID5B	1.000	0.120	10	62013280	intron variant	C/T	snv		0.37	1
rs7923074	ARID5B	1.000	0.120	10	61963681	intron variant	A/C	snv		0.56	1
rs141708090	C3orf20	1.000	0.120	3	14761602	missense variant	G/T	snv	1.9E-03	5.2E-04	1
rs2043211	CARD8	0.653	0.480	19	48234449	missense variant	A/T	snv	0.33	0.29	29
rs72772090	CAST	1.000	0.120	5	96700607	intron variant	G/A;C	snv			3
rs4617118	CCDC26	1.000	0.120	8	129143897	intron variant	A/C;G	snv		0.20	1
rs73195662	CDHR3	1.000	0.120	7	106018014	missense variant	C/A;G;T	snv	7.2E-02; 2.0E-05		1
rs3731217	CDKN2A	0.763	0.320	9	21984662	intron variant	A/C;T	snv			10
rs2069426	CDKN2B ; CDKN2B-AS1	1.000	0.120	9	22006274	intron variant	G/A;C;T	snv	4.4E-06; 4.4E-06; 7.5E-02		1
rs2239633	CEBPE	0.742	0.240	14	23119848	upstream gene variant	G/A	snv		0.38	12
rs8015478	CEBPE	1.000	0.120	14	23116809	downstream gene variant	A/C	snv		0.68	2