Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4246215
FADS2 ; FEN1
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv 29
rs174548
FADS2 ; FADS1
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 17
rs4666002
ZNF512
0.925 0.120 2 27617773 intron variant G/A;C snv 6
rs174455
FADS3
1.000 0.080 11 61888645 intron variant G/A;C snv 5
rs334809
IL5RA
0.925 0.080 3 3088537 intron variant A/G;T snv 4
rs11667159 19 46291989 intergenic variant C/A;T snv 3
rs11671710 19 46288677 regulatory region variant C/G;T snv 3
rs526126
FADS2
1.000 0.040 11 61857413 intron variant G/C;T snv 0.81; 8.0E-06 3
rs11230815 11 61868654 downstream gene variant G/C;T snv 2
rs149803
MYRF ; TMEM258
11 61771548 synonymous variant C/G;T snv 0.18 2
rs17156426
FADS2
11 61841851 intron variant A/G;T snv 2
rs174476
RAB3IL1
11 61906646 synonymous variant C/A;G;T snv 0.30 2
rs174585
FADS2
11 61844222 intron variant G/A;T snv 2
rs174591
FADS2
11 61850204 intron variant T/A;G snv 2
rs174597
FADS2
11 61853568 intron variant G/A;C;T snv 2
rs174634
MIR6746 ; FADS3
11 61879915 intron variant G/C;T snv 2
rs17764324
FADS2
11 61867616 downstream gene variant G/A;T snv 2
rs2727261
RAB3IL1
11 61944659 regulatory region variant T/C;G snv 2
rs4453795
FGF12
3 192376186 intron variant A/G;T snv 2
rs7104849 11 61870572 downstream gene variant G/A;T snv 2
rs7394871
FADS3
11 61885042 intron variant A/C;T snv 2
rs742614 20 33894826 intergenic variant A/G;T snv 2
rs7482316 11 61872726 downstream gene variant G/A;C snv 2
rs768116521
LOC105372112
18 49629266 TF binding site variant G/A;T snv 2
rs8523
ELOVL2
6 10980820 3 prime UTR variant G/A;C snv 2