Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
rs7103411
BDNF ; BDNF-AS
0.752 0.160 11 27678578 intron variant C/T snv 0.82 15
rs3791679
EFEMP1 ; LOC112268416
0.925 0.120 2 55869757 intron variant A/G snv 0.20 11
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 10
rs987237
TFAP2B
0.925 0.120 6 50835337 intron variant A/G snv 0.17 10
rs3751812
FTO
0.882 0.160 16 53784548 intron variant G/T snv 0.30 8
rs7647305
DGKG
1.000 0.080 3 186116501 intron variant T/C snv 0.74 8
rs10195252
COBLL1
0.925 0.080 2 164656581 intron variant T/C snv 0.48 7
rs2241423
MAP2K5
0.882 0.120 15 67794500 intron variant G/A snv 0.29 7
rs2710323
ITIH1
0.851 0.080 3 52781889 intron variant T/C snv 0.49 0.54 7
rs3817334
MTCH2
1.000 0.080 11 47629441 intron variant C/T snv 0.36 7
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 7
rs7531118
LOC105378797
1.000 0.080 1 72371556 intron variant T/C snv 0.40 7
rs7759938
LIN28B-AS1
0.925 0.120 6 104931079 intron variant C/T snv 0.62 7
rs849140
JAZF1
0.851 0.240 7 28144083 intron variant T/C snv 0.58 7
rs9930333
FTO
0.882 0.120 16 53766065 intron variant T/C;G snv 7
rs1812175
HHIP-AS1 ; HHIP
4 144653692 intron variant A/G snv 0.79 6
rs2030323
BDNF
0.925 0.080 11 27706992 intron variant A/C snv 0.83 6
rs395962
LIN28B
6 104949543 intron variant T/G snv 0.72 6
rs4788102
SH2B1
0.851 0.160 16 28862077 intron variant G/A snv 0.34 6
rs55872725
FTO
16 53775211 intron variant C/T snv 0.31 6
rs6976930
BAZ1B
0.925 0.120 7 73471480 intron variant G/A snv 0.23 6
rs7133378
DNAH10 ; CCDC92
12 123924955 intron variant G/A snv 0.38 6
rs718314
LOC105369705
0.882 0.120 12 26300350 intron variant A/G snv 0.27 6