Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs187238
IL18
0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs755622
MIF-AS1 ; MIF
0.611 0.720 22 23894205 intron variant G/C snv 0.26 44
rs12203592
IRF4
0.649 0.320 6 396321 intron variant C/T snv 0.10 38
rs10502861
SLC14A2
0.807 0.080 18 45220183 intron variant C/T snv 0.32 7
rs10888690
FAF1
0.807 0.080 1 50494849 intron variant T/A;C snv 7
rs111668293
TBX15
0.807 0.080 1 118896200 intron variant G/- del 0.12 7
rs115182912 0.807 0.080 3 126274431 intron variant G/A snv 1.5E-02 7
rs11593840
LRMDA
0.807 0.080 10 76436854 intron variant A/G snv 0.40 7
rs1160312
LINC01432
0.807 0.080 20 22069865 intron variant A/G snv 0.55 7
rs12214131 0.807 0.080 6 105760046 intron variant G/A snv 0.29 7
rs12565727
C1orf127
0.807 0.080 1 10973025 intron variant A/G snv 0.31 7
rs1262557 0.807 0.080 6 126733443 intron variant C/T snv 0.51 7
rs12702271 0.807 0.080 7 46904161 intron variant C/T snv 0.20 7
rs12902958
DRAIC
0.807 0.080 15 69747915 intron variant G/A snv 7.7E-02 7
rs13021718
DPY30 ; MEMO1
0.807 0.080 2 31956355 intron variant G/A snv 0.15 7
rs1422798
EBF1
0.807 0.080 5 158893869 intron variant C/G snv 0.32 7
rs1819008
LOC105373757
0.807 0.080 2 176833154 intron variant C/A;T snv 0.49 7
rs2073963
HDAC9
0.807 0.080 7 18838251 intron variant T/G snv 0.43 7
rs2095921
C1orf127
0.807 0.080 1 10973265 intron variant C/G;T snv 7
rs34800162
SLC14A2
0.807 0.080 18 45228094 intron variant T/G snv 0.32 7
rs35892873
KLF15
0.807 0.080 3 126350105 intron variant C/T snv 0.33 7
rs3781452
FAM53B
0.807 0.080 10 124666560 intron variant C/T snv 0.60 7
rs3781458
FAM53B
0.807 0.080 10 124655362 intron variant C/A;G;T snv 7
rs4690116
FGF5
0.807 0.080 4 80285223 intron variant T/A snv 0.59 7