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	AF GENOME	Num. diseases
rs25487	XRCC1	0.441	0.800	19	43551574	missense variant	T/C	snv	0.68	0.71	205
rs16754	WT1	0.732	0.240	11	32396399	synonymous variant	T/C	snv	0.24; 4.0E-06	0.17	15
rs1310678797	VDR	0.882	0.120	12	47857143	missense variant	C/T	snv		7.0E-06	3
rs1448674651	TYMS ; ENOSF1	0.667	0.560	18	671384	missense variant	G/A;C	snv	4.0E-06		23
rs1142345	TPMT	0.776	0.280	6	18130687	missense variant	T/C;G	snv	3.7E-02		9
rs143125661	TPMT	0.882	0.120	6	18149120	missense variant	C/T	snv	4.0E-06	7.0E-06	3
rs1800460	TPMT	0.807	0.320	6	18138997	missense variant	C/T	snv	2.8E-02	2.6E-02	7
rs1800462	TPMT	0.851	0.240	6	18143724	missense variant	C/G	snv	1.7E-03	2.0E-03	5
rs1042522	TP53	0.426	0.800	17	7676154	missense variant	G/C;T	snv	0.67		242
rs6589664	TMEM25	0.882	0.120	11	118534089	synonymous variant	G/A	snv	0.30	0.27	3
rs2742038	TLX1 ; TLX1NB	0.882	0.120	10	101137330	3 prime UTR variant	C/T	snv		0.16	3
rs80338880	TFR2	0.732	0.360	7	100633100	stop gained	G/C	snv		7.0E-06	12
rs4880	SOD2	0.500	0.840	6	159692840	missense variant	A/G	snv	0.48	0.47	131
rs4149009	SLCO1A2	0.882	0.120	12	21267537	3 prime UTR variant	C/T	snv		0.38	3
rs1051296	SLC19A1	0.882	0.120	21	45514947	3 prime UTR variant	A/C	snv	0.43	0.44	3
rs569954362	SLC19A1	0.851	0.160	21	45530871	synonymous variant	G/A	snv			4
rs1979277	SHMT1	0.620	0.560	17	18328782	missense variant	G/A	snv	0.27	0.31	45
rs12402181	SGIP1 ; MIR3117	0.882	0.120	1	66628488	mature miRNA variant	G/A	snv	0.17	0.24	3
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
rs6461639	RAPGEF5	0.882	0.120	7	22147337	intron variant	T/A;C	snv			3
rs397507520	PTPN11	0.658	0.520	12	112453279	missense variant	G/C;T	snv			39
rs885822	PRF1	0.882	0.120	10	70598821	missense variant	G/A;C	snv	0.64		3
rs6966	PPP1R13L	0.807	0.160	19	45379704	3 prime UTR variant	T/A;G	snv	0.18		6
rs9479	PML	0.851	0.120	15	74036235	3 prime UTR variant	A/G	snv		0.50	6