DisGeNET - a database of gene-disease associations

Source: GWASDB

Variants associated to the Disease: Serum total cholesterol measurement ×

Variants associated to the Gene: LIPC ×

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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
rs1800588	ALDH1A2 ; LIPC	0.790	0.200	15	58431476	intron variant	C/G;T	snv	0.30		6
rs261332	ALDH1A2 ; LIPC-AS1 ; LIPC	0.851	0.120	15	58435126	non coding transcript exon variant	A/G	snv		0.80	6
rs8033940	ALDH1A2 ; LIPC			15	58432643	intron variant	G/A	snv		0.41	5
rs8034802	ALDH1A2 ; LIPC			15	58432593	intron variant	T/A	snv		0.33	5
rs261336	ALDH1A2 ; LIPC ; LIPC-AS1			15	58450219	intron variant	G/A	snv		0.81	5
rs588136	ALDH1A2 ; LIPC ; LIPC-AS1			15	58438299	intron variant	C/G;T	snv			5
rs473224	LIPC-AS1 ; ALDH1A2 ; LIPC			15	58445142	intron variant	T/A;G	snv			5
rs261342	LIPC-AS1 ; LIPC ; ALDH1A2			15	58438954	intron variant	G/A;C;T	snv			5
rs2070895	LIPC ; ALDH1A2	0.807	0.120	15	58431740	intron variant	G/A	snv		0.33	5
rs485538	LIPC ; ALDH1A2 ; LIPC-AS1			15	58448978	intron variant	C/G;T	snv			5
rs485671	LIPC ; ALDH1A2 ; LIPC-AS1			15	58448935	intron variant	A/C;T	snv			5
rs261338	LIPC ; LIPC-AS1 ; ALDH1A2			15	58442806	intron variant	A/G	snv		0.83	5
rs6494005	ALDH1A2 ; LIPC	1.000	0.040	15	58432325	non coding transcript exon variant	A/G	snv		0.38	4
rs572410	LIPC-AS1 ; ALDH1A2 ; LIPC			15	58449185	intron variant	C/G;T	snv			4
rs11635491	LIPC ; ALDH1A2			15	58427542	intron variant	G/A	snv		0.27	4
rs261341	LIPC ; ALDH1A2 ; LIPC-AS1			15	58439368	intron variant	A/G	snv		0.54	4
rs1077835	ALDH1A2 ; LIPC			15	58431227	intron variant	A/G	snv		0.34	3
rs261334	LIPC ; ALDH1A2 ; LIPC-AS1			15	58434545	intron variant	G/C	snv		0.73	3
rs1077834	LIPC ; ALDH1A2			15	58431280	intron variant	T/C	snv		0.34	1