DisGeNET - a database of gene-disease associations

List of shared variants

Adult Acute Lymphocytic Leukemia, C0751606

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	Num. diseases
rs1039659576	MTR	0.689	0.520	1	236803473	missense variant	A/G	snv		21
rs1042522	TP53	0.426	0.800	17	7676154	missense variant	G/C;T	snv	0.67	242
rs1045642	ABCB1	0.456	0.840	7	87509329	synonymous variant	A/G;T	snv	0.50	214
rs104893636	HOXD4 ; HOXD3	0.882	0.120	2	176151875	missense variant	A/C;T	snv	5.2E-06; 7.9E-04	3
rs1057519743	CRLF2	0.827	0.120	Y	1196852	missense variant	A/C	snv		6
rs1057519866	NT5C2	0.851	0.120	10	103093198	missense variant	C/T	snv		5
rs10828317	PIP4K2A	0.776	0.280	10	22550699	missense variant	T/C	snv		9
rs111033563	LOC108783645 ; HFE	0.776	0.240	6	26092916	missense variant	A/C	snv	4.0E-06	8
rs1127354	ITPA	0.667	0.400	20	3213196	missense variant	C/A;G	snv	7.5E-02	26
rs1142345	TPMT	0.776	0.280	6	18130687	missense variant	T/C;G	snv	3.7E-02	9
rs1169704167	ATM	0.882	0.120	11	108284370	frameshift variant	-/T	delins	8.0E-06	3
rs1188383936	F2	0.524	0.760	11	46725976	missense variant	C/T	snv	8.0E-06	102
rs1194008138	NR3C1	0.882	0.120	5	143400121	missense variant	T/C	snv	4.0E-06	3
rs1206846668	FOLH1	0.724	0.400	11	49185773	missense variant	G/A	snv	4.1E-06	16
rs121913459	ABL1	0.672	0.160	9	130872896	missense variant	C/T	snv		25
rs1275561861	HLA-A	0.672	0.360	6	29944350	missense variant	G/A	snv		23
rs1296957097	CHEK2	0.882	0.120	22	28719401	missense variant	A/G	snv		3
rs1427331568	NR3C1	0.882	0.120	5	143314010	missense variant	G/C	snv		3
rs1448674651	TYMS ; ENOSF1	0.667	0.560	18	671384	missense variant	G/A;C	snv	4.0E-06	23
rs17069665	FOXO3	0.882	0.120	6	108620265	intron variant	A/C;G	snv		4
rs17855750	IL27	0.695	0.480	16	28503907	missense variant	A/C;T	snv	6.4E-02; 4.0E-06	21
rs200378616	ABCB1	0.882	0.120	7	87544938	missense variant	G/C;T	snv	4.0E-05; 8.0E-06	3
rs200928781	CHEK2	0.752	0.240	22	28695800	missense variant	T/A;C;G	snv	2.4E-05	11
rs2069727	IFNG ; IFNG-AS1	0.763	0.320	12	68154443	intron variant	T/A;C	snv		9
rs2295080	MTOR	0.695	0.320	1	11262571	upstream gene variant	G/C;T	snv		20