Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3126085
FLG-AS1
0.851 0.280 1 152328341 intron variant G/A snv 0.29 5
rs941934
FLG-AS1
0.851 0.200 1 152417976 intron variant T/A;C snv 5
rs1700159
ACVRL1
1.000 0.040 12 51912002 intron variant C/A;G;T snv 4
rs1870940
ZBTB7B
0.851 0.080 1 155011887 intron variant G/A snv 0.22 4
rs334809
IL5RA
0.925 0.080 3 3088537 intron variant A/G;T snv 4
rs4572450
ZNF652
0.882 0.120 17 49343367 intron variant T/C snv 0.78 4
rs4722404 0.851 0.120 7 3089155 intron variant T/C snv 0.40 4
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
rs114269697
JAK1
1.000 0.040 1 64848529 intron variant C/A snv 7.3E-03 3
rs115288876
LOC105371442
0.925 0.120 1 152027641 intron variant G/A snv 2.5E-02 3
rs117137535
ARRDC1
0.882 0.120 9 137605991 intron variant G/A snv 2.7E-02 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
rs35441874
CLEC16A
0.882 0.120 16 11119164 intron variant T/A snv 0.19 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
rs4739738 0.882 0.120 8 80379410 intron variant G/A snv 0.60 3
rs56375023
SMAD3
0.925 0.120 15 67156025 intron variant G/A snv 0.17 3
rs574456
LRP1B
0.882 0.160 2 140644133 intron variant A/T snv 8.1E-02 3
rs7518129
TNFSF4
0.882 0.120 1 173194429 intron variant A/G snv 0.47 3
rs10245867
JAZF1
0.925 0.080 7 28102567 intron variant G/T snv 0.37 2