Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6765789
TGM4
3 44897094 intron variant A/C snv 1.00 1
rs10897203 11 62011041 downstream gene variant A/C snv 0.99 1
rs495806
LIPC ; ALDH1A2
15 58426498 intron variant C/A snv 0.98 1
rs3019619 11 62039499 intergenic variant T/A snv 0.98 1
rs557108
ALDH1A2
15 58349112 intron variant C/T snv 0.96 1
rs9359145
MYO6
6 75878473 intron variant G/A snv 0.95 1
rs1023616 5 164177605 intron variant T/C snv 0.94 1
rs4321764 5 164171602 intron variant G/A snv 0.94 1
rs1017217 5 164176197 intron variant G/A snv 0.94 1
rs1895305 5 164181111 intron variant C/T snv 0.94 1
rs6591668
FADS3
11 61893641 upstream gene variant T/C snv 0.94 1
rs207129 1 55349235 intron variant A/G snv 0.94 1
rs2072560
ZPR1 ; APOA5
11 116791110 missense variant T/C snv 0.89 0.94 5
rs207155 1 55339229 intron variant T/C snv 0.93 1
rs6589565
BUD13
11 116769521 intron variant A/G snv 0.93 5
rs10790162
BUD13
0.882 0.160 11 116768388 intron variant A/G;T snv 0.93 7
rs7350481 0.882 0.040 11 116715567 regulatory region variant T/C snv 0.93 8
rs2266788
APOA5 ; ZPR1
0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 19
rs1558860 11 116736652 regulatory region variant A/C snv 0.93 1
rs9326246 0.925 0.040 11 116741017 intergenic variant C/G snv 0.93 9
rs7432026 3 88562447 intergenic variant A/C snv 0.93 1
rs7614273 3 88542677 intergenic variant T/C snv 0.93 1
rs9878827 3 88548089 intergenic variant T/G snv 0.93 1
rs6419877 3 88560317 intergenic variant A/G snv 0.93 1
rs3957559
MYH15
3 108466011 intron variant T/C snv 0.92 1