DisGeNET - a database of gene-disease associations

List of associated variants

Adult Acute Lymphocytic Leukemia, C0751606

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
rs10994982	ARID5B	0.790	0.120	10	61950345	intron variant	A/G	snv		0.49	7
rs3135388	HLA-DRA	0.807	0.240	6	32445274	downstream gene variant	A/G	snv		0.90	7
rs9479	PML	0.851	0.120	15	74036235	3 prime UTR variant	A/G	snv		0.50	6
rs4748793		0.851	0.120	10	22194082	intergenic variant	A/G	snv		0.18	4
rs6964969	IKZF1	0.851	0.120	7	50405553	downstream gene variant	A/G	snv		0.23	4
rs1296957097	CHEK2	0.882	0.120	22	28719401	missense variant	A/G	snv			3
rs138047632	LOC107987304 ; SLC19A1	0.882	0.120	21	45525860	missense variant	A/G	snv	2.4E-03	2.2E-03	3
rs7809758	DDC ; FIGNL1	0.882	0.120	7	50505635	intron variant	A/G	snv		0.36	3
rs880028	FIGNL1 ; DDC	0.882	0.120	7	50502438	intron variant	A/G	snv		0.21	3
rs1045642	ABCB1	0.456	0.840	7	87509329	synonymous variant	A/G;T	snv	0.50		214
rs2043211	CARD8	0.653	0.480	19	48234449	missense variant	A/T	snv	0.33	0.29	29
rs6021191	NFATC2	0.851	0.120	20	51419700	intron variant	A/T	snv		4.9E-02	5
rs1470755915	RUNX1T1	0.776	0.240	8	92005229	missense variant	C/A	snv		7.0E-06	10
rs927698341	RUNX1T1	0.776	0.240	8	92005280	synonymous variant	C/A	snv	4.0E-06	2.8E-05	10
rs7088318	PIP4K2A	0.851	0.120	10	22564019	intron variant	C/A	snv		0.55	4
rs1127354	ITPA	0.667	0.400	20	3213196	missense variant	C/A;G	snv	7.5E-02		26
rs200890679	MTHFR	0.790	0.240	1	11795191	missense variant	C/A;G	snv	1.8E-04	2.0E-04	7
rs9400241	FOXO3	0.882	0.120	6	108682786	3 prime UTR variant	C/A;G	snv			4
rs41320251	ITPA	0.882	0.120	20	3213196	missense variant	C/A;G	snv			3
rs3731249	CDKN2A	0.683	0.320	9	21970917	missense variant	C/A;G;T	snv	2.1E-02		23
rs35201683	HFE	0.732	0.360	6	26094205	stop gained	C/A;T	snv	1.4E-03		12
rs3824662	GATA3	0.752	0.320	10	8062245	intron variant	C/A;T	snv			11
rs757891309	MTR	0.882	0.120	1	236850389	missense variant	C/A;T	snv	4.0E-06; 4.0E-06		4
rs2910164	MIR3142HG ; MIR146A	0.447	0.880	5	160485411	mature miRNA variant	C/G	snv	0.71; 4.1E-06	0.70	193
rs1805794	NBN	0.605	0.600	8	89978251	missense variant	C/G	snv	0.35	0.31	41