Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2427827
FCER1A
1.000 0.120 1 159302021 intron variant T/C snv 0.65 2
rs1420101
IL1RL1 ; IL18R1
0.827 0.280 2 102341256 synonymous variant C/T snv 0.33 0.35 8
rs4150407
ERCC3
1.000 0.120 2 127292055 3 prime UTR variant T/C snv 0.47 3
rs6543124
IL18R1
1.000 0.120 2 102370999 intron variant T/A snv 0.44 1
rs828618
DCBLD2
0.925 0.160 3 98822789 intron variant G/A snv 0.28 0.22 2
rs17718444
FOXP1
1.000 0.120 3 71450250 intron variant C/T snv 0.27 1
rs1050152
SLC22A4 ; MIR3936HG
0.776 0.480 5 132340627 missense variant C/T snv 0.29 0.28 10
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 10
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs3129878
HLA-DRA
0.807 0.360 6 32440958 intron variant A/C snv 0.30 6
rs2428494
HLA-B
0.827 0.160 6 31354420 intron variant T/A;C snv 5
rs28383314 0.925 0.160 6 32619436 regulatory region variant T/C snv 0.61 5
rs9268644
HLA-DRA
0.827 0.360 6 32440267 intron variant A/C snv 0.68 5
rs1391371
HLA-DQA1
0.925 0.160 6 32636021 intron variant A/C;T snv 2
rs62408225
BACH2
1.000 0.120 6 90246690 intron variant A/G snv 0.26 2
rs74767530
CFTR
0.851 0.320 7 117627537 stop gained C/T snv 5.6E-05 4.9E-05 5
rs3807213
IFRD1
0.882 0.200 7 112465699 intron variant G/T snv 0.57 3
rs7817
IFRD1
0.925 0.200 7 112475603 3 prime UTR variant C/G;T snv 2
rs3939286 0.776 0.360 9 6210099 regulatory region variant T/A;C snv 12
rs1888909 0.882 0.200 9 6197392 downstream gene variant T/A;C snv 4
rs1444782 0.851 0.240 10 9016708 intergenic variant G/A snv 0.35 5
rs10905284
GATA3
0.882 0.200 10 8073399 intron variant C/A;T snv 4
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 19
rs113795008
BET1L ; SCGB1C1
1.000 0.120 11 192836 intron variant A/G snv 0.17 1
rs2280540
BET1L ; SCGB1C1
1.000 0.120 11 192997 intron variant G/A;C;T snv 1