DisGeNET - a database of gene-disease associations

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Variants associated to the Gene: ELOVL2-AS1 ×

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DSI _v

DPI _v

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Consequence

AF_EXOME

AF_GENOME

Variant	Gene	DSI _v	DPI _v	Chr	Position	Consequence	Alleles	Class	AF EXOME	AF GENOME	Num. diseases
rs9393903	ELOVL2 ; ELOVL2-AS1			6	11042676	intron variant	G/A	snv		0.18	3
rs9468304	ELOVL2-AS1 ; ELOVL2	1.000	0.040	6	11041932	intron variant	G/A	snv		0.19	2
rs12662634	ELOVL2-AS1			6	11073958	intron variant	G/A	snv		0.17	1
rs1321535	ELOVL2-AS1			6	11075793	intron variant	T/G	snv		0.41	1
rs17675322	ELOVL2-AS1			6	11058952	intron variant	T/A	snv		0.59	1
rs17764682	ELOVL2-AS1			6	11058582	intron variant	A/C	snv		0.24	1
rs2147041	ELOVL2-AS1			6	11050290	intron variant	A/G	snv		0.53	1
rs4711170	ELOVL2-AS1			6	11070201	intron variant	C/A	snv		0.17	1
rs4711171	ELOVL2-AS1			6	11074114	intron variant	C/A;T	snv			1
rs4713165	ELOVL2-AS1			6	11074069	intron variant	T/C	snv		0.41	1
rs6900220	ELOVL2-AS1			6	11064905	intron variant	T/C	snv		0.53	1
rs9368564	ELOVL2-AS1			6	11060050	intron variant	A/G;T	snv			1
rs9393915	ELOVL2-AS1			6	11072089	intron variant	C/T	snv		0.23	1
rs9295763	ELOVL2-AS1 ; ELOVL2			6	11044959	non coding transcript exon variant	G/A;C;T	snv			1
rs9295764	ELOVL2 ; ELOVL2-AS1			6	11044963	non coding transcript exon variant	A/G	snv		0.59	1