Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9357733
EFHC1
0.851 0.160 6 52427338 intron variant A/G snv 0.19 4
rs976078 0.882 0.120 13 82963398 intron variant A/C snv 0.15 4
rs10791824
OVOL1-AS1 ; OVOL1
0.882 0.160 11 65791795 intron variant A/G;T snv 3
rs13015714
IL18R1
0.882 0.200 2 102355405 intron variant G/T snv 0.77 3
rs13139310
IRF2
0.925 0.120 4 184435757 intron variant G/A;C snv 3
rs13360927
TMEM232
0.882 0.160 5 110700055 intron variant A/G snv 9.3E-02 3
rs13361382
TMEM232
0.882 0.160 5 110713253 intron variant G/A snv 9.3E-02 3
rs2251746
FCER1A
0.882 0.120 1 159302270 intron variant T/C snv 0.20 3
rs360721
IL18
0.882 0.200 11 112155193 intron variant G/A;C snv 3
rs438421
IL12RB1
0.882 0.200 19 18065276 intron variant A/G;T snv 3
rs574456
LRP1B
0.882 0.160 2 140644133 intron variant A/T snv 8.1E-02 3
rs11079788
TBX21
0.925 0.120 17 47743357 intron variant C/T snv 0.23 2
rs11150780
SLC38A10
0.925 0.120 17 81290360 intron variant A/G;T snv 2
rs11167761
PCDH1
0.925 0.120 5 141858778 intron variant G/A snv 0.14 2
rs11204971
FLG-AS1
0.925 0.120 1 152286602 intron variant A/G snv 0.15 2
rs1422985
SPINK5
0.925 0.120 5 148114596 intron variant A/C snv 3.2E-02 2
rs17718511
SPINK5
0.925 0.120 5 148072009 intron variant A/G snv 3.2E-02 2
rs2059876
CHST8
0.925 0.120 19 33639430 intron variant C/T snv 0.28 2
rs2066446
IL12RB2
0.925 0.120 1 67315434 intron variant A/G snv 0.20 2
rs224108 0.925 0.120 10 62789851 intron variant T/C;G snv 0.21 2
rs2533291
PTPRN2
0.925 0.120 7 157712962 intron variant C/T snv 0.12 2
rs2897442
KIF3A
0.925 0.120 5 132713335 intron variant C/A;T snv 2
rs2944542
ZNF365
0.925 0.120 10 62610240 intron variant C/G snv 0.71 2
rs3219177
RETN
0.925 0.120 19 7669483 intron variant C/T snv 0.20 0.19 2
rs3756094
IRF2
0.925 0.120 4 184429780 intron variant A/G snv 0.66 2