DisGeNET - a database of gene-disease associations

Source: ALL

Variants associated to the Gene: MYC ×

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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
rs756091827	MYC ; CASC11	0.851	0.200	8	127738435	missense variant	C/G;T	snv			6
rs1057519918	CASC11 ; MYC	0.851	0.200	8	127738390	missense variant	C/T	snv			5
rs750664148	CASC11 ; MYC	0.851	0.200	8	127738434	missense variant	A/C;G	snv			5
rs4645959	CASC11 ; MYC	0.882	0.080	8	127738294	missense variant	A/C;G	snv	1.6E-05; 2.3E-02		3
rs747141352	CASC11 ; MYC	0.882	0.160	8	127736607	missense variant	G/A;C	snv	8.0E-06		3
rs2071346	MYC ; CASC11	0.925	0.160	8	127736777	intron variant	G/T	snv		7.1E-02	3
rs4645948	MYC ; CASC11	0.882	0.160	8	127736252	synonymous variant	C/T	snv		2.8E-02	3
rs3824120	CASC11 ; MYC			8	127735707	missense variant	G/A;C;T	snv			2
rs121918683	MYC ; CASC11	1.000	0.160	8	127738519	missense variant	A/C	snv			2
rs28933407	MYC ; CASC11	1.000	0.160	8	127738431	missense variant	C/T	snv			2
rs1057519849	CASC11 ; MYC			8	127738386	missense variant	C/T	snv			1
rs1057519850	CASC11 ; MYC			8	127738447	missense variant	C/T	snv			1
rs121918685	CASC11 ; MYC	1.000	0.160	8	127738437	missense variant	C/G	snv			1
rs775522201	CASC11 ; MYC			8	127738393	missense variant	C/T	snv			1
rs1057519851	MYC			8	127738995	missense variant	C/G	snv			1
rs2070583	MYC	1.000	0.040	8	127741008	3 prime UTR variant	A/G	snv	4.2E-02	2.9E-02	1
rs117856857	MYC ; CASC11	1.000	0.080	8	127736248	missense variant	C/G	snv		1.7E-02	1