DisGeNET - a database of gene-disease associations

Source: ALL

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
rs1000778	FADS3	1.000	0.040	11	61887833	intron variant	A/G	snv		0.59	3
rs10468017	ALDH1A2	0.851	0.120	15	58386313	intron variant	C/T	snv		0.24	12
rs108499	TMEM258 ; MYRF			11	61779765	intron variant	C/T	snv		0.27	2
rs1535	FADS2	0.752	0.240	11	61830500	intron variant	A/G	snv		0.31	24
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	3
rs174455	FADS3	1.000	0.080	11	61888645	intron variant	G/A;C	snv			5
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
rs174479	RAB3IL1			11	61911282	intron variant	C/G	snv		0.17	2
rs174528	TMEM258 ; MYRF	1.000	0.080	11	61776027	intron variant	T/C	snv	0.42	0.42	5
rs174532	TMEM258 ; MYRF			11	61781402	intron variant	G/A	snv		0.20	2
rs174541	FADS2	1.000	0.080	11	61798436	intron variant	T/C	snv		0.29	8
rs174547	FADS2 ; FADS1	0.742	0.240	11	61803311	intron variant	T/C	snv		0.28	33
rs174556	FADS2 ; FADS1	0.925	0.160	11	61813163	intron variant	C/T	snv		0.26	7
rs174570	FADS2	0.882	0.200	11	61829740	intron variant	C/T	snv		0.15	11
rs174574	FADS2	1.000	0.080	11	61832870	intron variant	A/C	snv		0.55	7
rs174575	FADS2	1.000	0.040	11	61834531	intron variant	C/G	snv		0.25	3
rs174579	FADS2			11	61838141	intron variant	C/T	snv		0.16	2
rs174583	FADS2	0.807	0.320	11	61842278	intron variant	C/T	snv		0.35	16
rs174585	FADS2			11	61844222	intron variant	G/A;T	snv			2
rs174591	FADS2			11	61850204	intron variant	T/A;G	snv			2