Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 24
rs174583
FADS2
0.807 0.320 11 61842278 intron variant C/T snv 0.35 16
rs603424
PKD2L1
1.000 0.080 10 100315722 intron variant G/A snv 0.34 13
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24 12
rs174570
FADS2
0.882 0.200 11 61829740 intron variant C/T snv 0.15 11
rs174541
FADS2
1.000 0.080 11 61798436 intron variant T/C snv 0.29 8
rs4775041
ALDH1A2
1.000 0.040 15 58382496 intron variant G/C snv 0.24 8
rs174556
FADS2 ; FADS1
0.925 0.160 11 61813163 intron variant C/T snv 0.26 7
rs174574
FADS2
1.000 0.080 11 61832870 intron variant A/C snv 0.55 7
rs968567
FADS2 ; FADS1
0.851 0.240 11 61828092 intron variant C/T snv 0.11 7
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
rs174528
TMEM258 ; MYRF
1.000 0.080 11 61776027 intron variant T/C snv 0.42 0.42 5
rs2851682
FADS2
11 61848540 intron variant A/G snv 9.9E-02 5
rs2072114
FADS2
1.000 0.080 11 61837743 intron variant A/G snv 0.19 0.16 4
rs334809
IL5RA
0.925 0.080 3 3088537 intron variant A/G;T snv 4
rs3756963
ELOVL2
0.882 0.200 6 11021921 intron variant T/C snv 0.24 4
rs1000778
FADS3
1.000 0.040 11 61887833 intron variant A/G snv 0.59 3
rs10498676
ELOVL2
0.925 0.040 6 11026766 intron variant G/A snv 0.18 3
rs1077989
GPHN ; TMEM229B
1.000 0.080 14 67509105 intron variant A/C snv 0.39 3
rs174450
FADS3
1.000 0.080 11 61874070 intron variant G/T snv 0.44 3
rs174575
FADS2
1.000 0.040 11 61834531 intron variant C/G snv 0.25 3