DisGeNET - a database of gene-disease associations

List of associated variants

Phospholipid measurement, C0202177

Source: GWASDB ×

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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 GENOME	Num. diseases
rs780094	GCKR	0.658	0.400	2	27518370	intron variant	T/C	snv	0.67	24
rs780093	GCKR	0.763	0.240	2	27519736	intron variant	T/C	snv	0.68	13
rs10468017	ALDH1A2	0.851	0.120	15	58386313	intron variant	C/T	snv	0.24	10
rs1535	FADS2	0.752	0.240	11	61830500	intron variant	A/G	snv	0.31	10
rs174547	FADS2 ; FADS1	0.742	0.240	11	61803311	intron variant	T/C	snv	0.28	10
rs174570	FADS2	0.882	0.200	11	61829740	intron variant	C/T	snv	0.15	10
rs4775041	ALDH1A2	1.000	0.040	15	58382496	intron variant	G/C	snv	0.24	7
rs4666002	ZNF512	0.925	0.120	2	27617773	intron variant	G/A;C	snv		6
rs174583	FADS2	0.807	0.320	11	61842278	intron variant	C/T	snv	0.35	5
rs2851682	FADS2			11	61848540	intron variant	A/G	snv	9.9E-02	5
rs174541	FADS2	1.000	0.080	11	61798436	intron variant	T/C	snv	0.29	4
rs603424	PKD2L1	1.000	0.080	10	100315722	intron variant	G/A	snv	0.34	4
rs174455	FADS3	1.000	0.080	11	61888645	intron variant	G/A;C	snv		3
rs174556	FADS2 ; FADS1	0.925	0.160	11	61813163	intron variant	C/T	snv	0.26	3
rs9393903	ELOVL2 ; ELOVL2-AS1			6	11042676	intron variant	G/A	snv	0.18	3
rs968567	FADS2 ; FADS1	0.851	0.240	11	61828092	intron variant	C/T	snv	0.11	3
rs1000778	FADS3	1.000	0.040	11	61887833	intron variant	A/G	snv	0.59	2
rs108499	TMEM258 ; MYRF			11	61779765	intron variant	C/T	snv	0.27	2
rs17156426	FADS2			11	61841851	intron variant	A/G;T	snv		2
rs17156442	FADS2			11	61846551	intron variant	C/T	snv	0.11	2
rs174450	FADS3	1.000	0.080	11	61874070	intron variant	G/T	snv	0.44	2
rs174456	FADS3			11	61888710	intron variant	C/A	snv	0.59	2
rs174464	FADS3			11	61890454	intron variant	A/G	snv	0.59	2
rs174472	RAB3IL1			11	61904484	intron variant	A/G	snv	0.41	2
rs174478	RAB3IL1			11	61911104	intron variant	T/G	snv	0.31	2