DisGeNET - a database of gene-disease associations

Source: GWASCAT

Variants associated to the Gene: CPED1 ×

Results per page

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
rs13245690	CPED1			7	121145010	intron variant	A/G	snv		0.32	2
rs6950680	CPED1			7	121150233	intron variant	A/G	snv		0.32	1
rs2110281	CPED1			7	121085755	intron variant	G/A	snv		0.31	1
rs9640799	CPED1			7	121190161	intron variant	A/G	snv		0.62	1
rs35789132	CPED1			7	121163232	intron variant	A/G	snv		0.30	1
rs13223036	CPED1			7	121107254	intron variant	T/G	snv		0.29	1
rs4609139	CPED1			7	121263761	intron variant	A/T	snv		0.31	1
rs67991850	CPED1			7	121173866	intron variant	C/A;T	snv			1
rs34249834	CPED1			7	121134062	intron variant	C/A	snv		0.34	1
rs798943	CPED1			7	121118845	intron variant	G/A	snv		0.35	1
rs10261386	CPED1	1.000	0.080	7	121071801	intron variant	C/T	snv		0.38	1
rs6942652	CPED1			7	121249218	intron variant	G/C;T	snv			1
rs2222543	CPED1			7	121262131	intron variant	G/C	snv		0.38	1
rs4731009	CPED1			7	121264763	intron variant	C/T	snv		0.38	1
rs77670845	CPED1			7	121229508	intron variant	ATGAA/-	delins		0.45	1