Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13125101 4 80253438 TF binding site variant G/A snv 0.24 6
rs13149993 4 80237391 regulatory region variant G/A;C snv 6
rs1495743 8 18415790 intergenic variant G/A;C snv 6
rs2643826 3 27521497 upstream gene variant C/T snv 0.56 6
rs35444 12 115114632 intergenic variant A/G snv 0.38 6
rs9292468 5 32818967 intergenic variant T/A;C snv 6
rs17035646
CASZ1
1 10736490 intron variant G/A;T snv 6
rs10255839
EVX1
7 27249498 intron variant G/A snv 0.87 6
rs55872725
FTO
16 53775211 intron variant C/T snv 0.31 6
rs7209400
LOC102724596
1.000 0.040 17 49372695 intron variant C/T snv 0.47 6
rs2156552
LOC105372112
1.000 0.040 18 49655298 downstream gene variant A/G;T snv 6
rs1290784
MECOM
3 169379112 intron variant C/A;T snv 6
rs2642438
MTARC1
1 220796686 missense variant A/G snv 0.75 0.78 6
rs62434129
PLEKHG1
6 150687701 intron variant A/G;T snv 8.8E-02 6
rs34311866
TMEM175
0.882 0.080 4 958159 missense variant T/C snv 0.18 0.14 6
rs10184428 2 164155317 intron variant C/A;G snv 5
rs11513729 1.000 0.080 12 111835695 downstream gene variant C/T snv 0.29 5
rs13209747 6 126794309 intron variant C/G;T snv 0.36 5
rs2013002 12 111762346 intron variant T/A;C snv 5
rs35225200 1.000 0.040 4 102225731 intergenic variant A/C snv 5.4E-02 5
rs35441 12 115115310 intergenic variant C/T snv 0.40 5
rs35443 12 115115073 intergenic variant G/C snv 0.40 5
rs509728 11 116662450 downstream gene variant G/C snv 2.7E-02 5
rs6108787 20 10986566 intron variant T/G snv 0.46 5
rs11066015
ACAD10
0.925 0.120 12 111730205 intron variant G/A snv 5.9E-03 5