Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35761398
CNR2
0.701 0.520 1 23875429 missense variant TT/CC mnv 19
rs879761216
CNR2
0.732 0.480 1 23875429 frameshift variant TT/C;T delins 14
rs71559680 0.827 0.120 6 21430497 intergenic variant TAG/CAT mnv 6
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs7517847
IL23R ; C1orf141
0.689 0.600 1 67215986 intron variant T/G snv 0.37 19
rs11465804
IL23R
0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 10
rs7192
HLA-DRA
0.827 0.200 6 32443869 missense variant T/G snv 0.64 0.61 7
rs1569414
FAM118A
0.807 0.160 22 45331684 intron variant T/G snv 0.44 6
rs34779708
CREM
0.827 0.120 10 35177257 intron variant T/G snv 0.33 6
rs3776414
DAP
0.827 0.120 5 10689450 intron variant T/G snv 0.48 6
rs4243971 0.827 0.120 20 32261714 intergenic variant T/G snv 0.64 6
rs111305875 0.827 0.120 6 167098098 intron variant T/G snv 3.0E-02 5
rs12987977
IL18R1
0.827 0.120 2 102358876 intron variant T/G snv 0.31 5
rs6425143 0.827 0.120 1 172875212 intron variant T/G snv 0.34 5
rs17234657 0.882 0.120 5 40401407 intergenic variant T/G snv 0.14 3
rs2189234
TET2
1.000 0.040 4 105154341 intron variant T/G snv 0.62 3
rs10185424 0.925 0.040 2 102046427 intron variant T/G snv 0.62 2
rs1127233
MUC13
0.925 0.040 3 124908177 missense variant T/G snv 0.24 0.26 2
rs11083840
PTGIR
1.000 0.040 19 46616653 downstream gene variant T/G snv 0.44 1
rs1440088
PLCL1
1.000 0.040 2 198006693 intron variant T/G snv 0.21 1
rs17188113
TRIM10 ; TRIM15
1.000 0.040 6 30163346 5 prime UTR variant T/G snv 0.13 1
rs2777491
RTF1
1.000 0.040 15 41443512 intron variant T/G snv 0.35 1
rs6088765
MMP24-AS1-EDEM2 ; MMP24OS ; PROCR
1.000 0.040 20 35211477 intron variant T/G snv 0.54 1
rs7911117 1.000 0.040 10 26890667 regulatory region variant T/G snv 0.18 1