Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7528684
FCRL3
0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 13
rs2227284
IL4
0.732 0.480 5 132677033 intron variant T/C;G snv 12
rs4143094
GATA3
0.752 0.240 10 8047173 intron variant T/G snv 0.70 12
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 12
rs8076131
ORMDL3
0.790 0.200 17 39924659 intron variant G/A;C snv 11
rs4794820
LRRC3C
0.790 0.160 17 39933091 intron variant A/G;T snv 9
rs1234314
TNFSF4
0.790 0.320 1 173208253 upstream gene variant C/A;G snv 7
rs2030519
LPP
0.827 0.200 3 188402113 intron variant G/A snv 0.61 7
rs1234315
TNFSF4
0.807 0.400 1 173209324 upstream gene variant C/T snv 0.57 6
rs2254546 0.807 0.400 8 11486171 upstream gene variant A/G snv 0.83 6
rs7936323 0.882 0.160 11 76582714 intergenic variant G/A snv 0.44 6
rs1600249
BLK
0.827 0.280 8 11502129 intron variant G/T snv 0.23 5
rs2428494
HLA-B
0.827 0.160 6 31354420 intron variant T/A;C snv 5
rs1310182
AP4B1-AS1 ; PTPN22
0.882 0.360 1 113830881 intron variant A/C;G snv 0.56 4
rs1438673 0.882 0.120 5 111131801 downstream gene variant C/T snv 0.61 4
rs17294280
SMAD3
0.882 0.120 15 67175947 intron variant A/G snv 0.19 4
rs231725 0.851 0.240 2 203875952 downstream gene variant G/A snv 0.38 4
rs428253
EBI3
0.851 0.200 19 4229916 intron variant G/C snv 0.33 4
rs4982958 0.851 0.200 14 24518659 intergenic variant C/T snv 0.50 4
rs7130588 0.882 0.200 11 76559639 regulatory region variant A/G snv 0.29 4
rs10519067
RORA
0.925 0.120 15 60776148 intron variant G/A snv 0.20 3
rs17513503 0.882 0.120 5 110810746 intergenic variant C/A;G snv 3
rs2164068
PLCL1
1.000 0.120 2 198079128 intron variant T/A snv 0.52 3
rs2289276
TSLP
0.882 0.160 5 111071809 5 prime UTR variant C/T snv 0.27 3
rs310241
JAK1
0.882 0.360 1 64837655 intron variant A/G snv 0.37 3