Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 28
rs34517439
DNAJB4 ; GIPC2
0.882 0.120 1 77984833 intron variant C/A snv 7.3E-02 7
rs754388
RIN3
0.882 0.120 14 92649065 intron variant G/C;T snv 7
rs113191842
FTO
16 53783406 intron variant G/A snv 9.4E-02 5
rs2812208
DLEU1
13 50132951 intron variant G/A;C snv 5
rs9936385
FTO
0.925 0.120 16 53785257 intron variant T/C snv 0.41 5
rs4800148
CABLES1
18 23144364 intron variant G/A;C snv 4
rs4870941 8 125486586 intron variant G/C snv 0.20 4
rs7223535
ATAD5
1.000 0.080 17 30884649 intron variant G/A snv 0.25 4
rs9388490
CENPW
1.000 0.080 6 126383649 intron variant C/T snv 0.42 4
rs11030119
BDNF
11 27706555 intron variant G/A;T snv 3
rs12513481
AP3B1
5 78155004 intron variant G/C snv 0.19 3
rs13245690
CPED1
7 121145010 intron variant A/G snv 0.32 3
rs35506085
IGF2 ; INS-IGF2 ; IGF2-AS
11 2144346 intron variant G/A snv 0.17 3
rs3818416
EDNRB-AS1 ; EDNRB
1.000 0.080 13 77900333 intron variant A/C snv 0.75 3
rs41271299
ID4
6 19839184 intron variant C/A;G;T snv 3
rs5750823
TAB1 ; LOC100506472
22 39433968 intron variant C/T snv 0.70 3
rs6570509
ADGRG6
6 142395149 intron variant G/T snv 0.41 3
rs72656010
PLAG1 ; CHCHD7
8 56209656 intron variant T/C snv 0.10 3
rs7996639
HS6ST3
13 96366836 intron variant G/A snv 0.50 3
rs917727
FAM3C
7 121378525 intron variant C/A;T snv 0.33 3
rs11014285
PRTFDC1
10 24889935 intron variant G/A snv 0.11 2
rs115179432
LTBP1
2 33123612 intron variant A/G snv 5.6E-02 2
rs11855017
MAPKBP1
15 41803948 intron variant C/A snv 0.15 2
rs12284933
PPP6R3
11 68552021 intron variant G/A snv 0.23 2