Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4938723
MIR34C ; BTG4 ; MIR34B ; LOC728196
0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs755622
MIF-AS1 ; MIF
0.611 0.720 22 23894205 intron variant G/C snv 0.26 44
rs153109
IL27
0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs10821936
ARID5B
0.742 0.200 10 61963818 intron variant C/T snv 0.69 11
rs3824662
GATA3
0.752 0.320 10 8062245 intron variant C/A;T snv 11
rs3731217
CDKN2A
0.763 0.320 9 21984662 intron variant A/C;T snv 10
rs7089424
ARID5B
0.752 0.200 10 61992400 intron variant T/G snv 0.32 10
rs11978267
IKZF1
0.763 0.240 7 50398606 intron variant A/G snv 0.25 9
rs2290400
GSDMB
0.790 0.360 17 39909987 intron variant T/C snv 0.48 9
rs1966862
ARHGAP24
0.790 0.120 4 85766908 intron variant A/G snv 0.14 8
rs10740055
ARID5B
0.790 0.240 10 61958720 intron variant C/A snv 0.49 7
rs10994982
ARID5B
0.790 0.120 10 61950345 intron variant A/G snv 0.49 7
rs924607
LOC105374608 ; LOC100996325
0.851 0.120 5 609978 intron variant C/T snv 0.32 7
rs2036914
F11
0.882 0.160 4 186271327 intron variant T/C snv 0.57 5
rs6021191
NFATC2
0.851 0.120 20 51419700 intron variant A/T snv 4.9E-02 5
rs6479778
ARID5B
0.827 0.200 10 61929318 intron variant T/C;G snv 5
rs7073837
ARID5B
0.851 0.120 10 61940136 intron variant A/C snv 0.58 0.64 4
rs7088318
PIP4K2A
0.851 0.120 10 22564019 intron variant C/A snv 0.55 4
rs12540874
GRB10
0.882 0.280 7 50597225 intron variant A/C;G snv 3
rs147481775
DEPDC5
1.000 0.120 22 31829377 intron variant C/A snv 6.6E-03 3
rs34531324
LINC01411
1.000 0.120 5 174435441 intron variant A/T snv 0.16 3
rs3781093
GATA3
0.882 0.120 10 8059964 intron variant T/C snv 0.19 3
rs3794845
MBP
0.882 0.120 18 77002561 intron variant G/C snv 0.12 3
rs4245555
GRB10
1.000 0.120 7 50593712 intron variant T/C snv 0.32 3
rs4463516 1.000 0.120 9 32867483 intron variant G/C;T snv 3