Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260333 0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58 12
rs579383
MYRF ; TMEM258
11 61769111 intron variant G/A snv 0.58 2
rs174574
FADS2
1.000 0.080 11 61832870 intron variant A/C snv 0.55 7
rs4713103
SYCP2L
6 10968908 intron variant G/T snv 0.55 1
rs2295602
ELOVL2
6 11005609 intron variant T/C snv 0.57 0.54 1
rs174449 11 61872907 downstream gene variant G/A snv 0.54 2
rs1570069
ELOVL2
6 11017592 intron variant A/G snv 0.54 1
rs7743830
ELOVL2
6 11013987 intron variant A/G snv 0.54 1
rs13966
RAB3IL1
11 61897520 3 prime UTR variant T/C snv 0.53 1
rs6900220
ELOVL2-AS1
6 11064905 intron variant T/C snv 0.53 1
rs2147041
ELOVL2-AS1
6 11050290 intron variant A/G snv 0.53 1
rs3798707
ELOVL2
6 10991702 intron variant C/T snv 0.53 1
rs12587311 14 28647489 intergenic variant T/C snv 0.53 1
rs3845427 1 181293302 intergenic variant T/A snv 0.52 1
rs509360
MYRF ; TMEM258
11 61781087 intron variant A/G snv 0.61 0.52 3
rs3798711
ELOVL2
6 11002577 intron variant T/C snv 0.52 1
rs1424760 2 162925277 intergenic variant C/T snv 0.52 1
rs174616
FADS2
1.000 0.080 11 61861650 intron variant G/A snv 0.51 3
rs8012543 14 28618344 upstream gene variant G/A snv 0.50 1
rs7773173
SYCP2L
6 10956470 intron variant G/C snv 0.50 1
rs2391388
ALG14
1 95020269 intron variant A/C snv 0.49 2
rs174626 11 61869585 downstream gene variant G/A snv 0.48 2
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 18
rs198476
MYRF ; MYRF-AS1
11 61758258 intron variant G/A snv 0.46 1
rs198462
MYRF ; MYRF-AS1
11 61756647 intron variant G/A snv 0.46 1