Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 21
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 18
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 17
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 15
rs7498665
SH2B1
0.925 0.120 16 28871920 missense variant A/G;T snv 0.35 9
rs2568958
LOC105378797
0.882 0.160 1 72299433 intron variant G/A;C snv 8
rs9368222
CDKAL1
1.000 0.080 6 20686765 intron variant C/A;T snv 8
rs13130484 1.000 0.080 4 45173674 intergenic variant C/A;T snv 7
rs887912 1.000 0.080 2 59075742 intron variant T/C;G snv 6
rs3822072
FAM13A
4 88820118 intron variant G/A;C snv 5
rs4836133
LOC105379158 ; LINC02240
0.925 0.160 5 124996410 intron variant C/A;G;T snv 5
rs10458787 1.000 0.040 10 4613373 intergenic variant A/C;G snv 4
rs12463617 1.000 0.080 2 629244 regulatory region variant A/C;T snv 4
rs4715210 6 50929538 regulatory region variant C/G;T snv 4
rs4771122
MTIF3
1.000 0.080 13 27446043 intron variant G/A;C snv 4
rs10789336
LOC105378797
1 72372723 intron variant G/A;C snv 3
rs12597579 16 20246545 intergenic variant C/A;T snv 3
rs12964056 18 60006567 upstream gene variant A/G;T snv 3
rs17124318
LINC01739
1 63015059 intron variant C/A;G;T snv 3
rs4377469
CCK
3 42261582 intron variant G/A;T snv 3
rs4646949
TAF11 ; UHRF1BP1
6 34877672 3 prime UTR variant T/C;G snv 3
rs591120
CRYZL2P-SEC16B ; SEC16B
1 177933618 missense variant G/A;C snv 4.0E-06; 0.42 3
rs8182584
PEPD
19 33418804 intron variant T/C;G snv 3
rs8192472
CCK
3 42258378 intron variant C/G;T snv 3