DisGeNET - a database of gene-disease associations

List of shared variants

Acute lymphocytic leukemia, C0023449

Disease: Childhood Acute Lymphoblastic Leukemia

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
rs7039798	FPGS	0.882	0.120	9	127794947	intron variant	G/A;C	snv			3
rs7088318	PIP4K2A	0.851	0.120	10	22564019	intron variant	C/A	snv		0.55	4
rs724159947	ETV6	0.851	0.120	12	11869601	missense variant	C/T	snv			6
rs72481843	NR3C1	0.882	0.120	5	143300685	splice donor variant	C/G	snv			3
rs7286979	EP300	0.882	0.120	22	41102623	intron variant	G/A	snv		0.26	3
rs757874631	CBL	0.882	0.120	11	119278211	missense variant	T/A;C	snv			4
rs757891309	MTR	0.882	0.120	1	236850389	missense variant	C/A;T	snv	4.0E-06; 4.0E-06		4
rs759602460	CNDP2	0.882	0.120	18	74518552	missense variant	C/G	snv	1.6E-05; 4.0E-06		3
rs766916111	ITPA	0.882	0.120	20	3223452	missense variant	T/C	snv	4.0E-06	7.0E-06	3
rs768315648	NR3C1	0.882	0.120	5	143399830	missense variant	T/C	snv	1.2E-05		3
rs76996680	LEF1	0.882	0.120	4	108163665	missense variant	G/A	snv	1.0E-03	3.4E-04	3
rs772470710	NSD2	0.882	0.120	4	1961074	missense variant	G/A	snv	4.0E-06		3
rs777926364	CYP3A5 ; ZSCAN25	0.882	0.120	7	99664017	missense variant	C/T	snv	4.2E-06		3
rs7789635		0.882	0.120	7	50405912	downstream gene variant	T/C	snv		0.40	4
rs7809758	DDC ; FIGNL1	0.882	0.120	7	50505635	intron variant	A/G	snv		0.36	3
rs7853758	LOC105376116 ; SLC28A3	0.851	0.120	9	84286011	synonymous variant	G/A	snv	0.15	0.19	5
rs786205155	ETV6	0.882	0.120	12	11884481	missense variant	T/C	snv			4
rs880028	FIGNL1 ; DDC	0.882	0.120	7	50502438	intron variant	A/G	snv		0.21	3
rs885822	PRF1	0.882	0.120	10	70598821	missense variant	G/A;C	snv	0.64		3
rs924607	LOC105374608 ; LOC100996325	0.851	0.120	5	609978	intron variant	C/T	snv		0.32	7
rs9400241	FOXO3	0.882	0.120	6	108682786	3 prime UTR variant	C/A;G	snv			4
rs9479	PML	0.851	0.120	15	74036235	3 prime UTR variant	A/G	snv		0.50	6
rs11099592	HPSE	0.851	0.160	4	83309466	missense variant	T/C	snv	0.78	0.80	5
rs121913459	ABL1	0.672	0.160	9	130872896	missense variant	C/T	snv			25
rs569954362	SLC19A1	0.851	0.160	21	45530871	synonymous variant	G/A	snv			4