DisGeNET - a database of gene-disease associations

Source: GWASDB

Variants associated to the Gene: CUBN ×

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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
rs17139292	CUBN			10	16828081	intron variant	G/A	snv		1.9E-02	3
rs1891473	CUBN			10	16861081	intron variant	T/C	snv		0.19	2
rs1801222	CUBN	0.925	0.160	10	17114152	missense variant	A/G	snv	0.73	0.72	2
rs12257093	CUBN			10	17022992	intron variant	G/A	snv		1.9E-02	2
rs7898873	CUBN			10	16835081	missense variant	G/A;C	snv	4.0E-06; 1.8E-02		2
rs1801239	CUBN	0.827	0.160	10	16877053	missense variant	T/C;G	snv	8.9E-02; 8.0E-06		1
rs7921488	CUBN	1.000	0.080	10	17127078	intron variant	A/G	snv		0.90	1
rs11254327	CUBN			10	17006709	intron variant	C/T	snv		0.40	1
rs11254363	CUBN	1.000	0.040	10	17088694	intron variant	A/G	snv		0.26	1