Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs759412116
ERCC2
0.581 0.640 19 45352210 missense variant C/G;T snv 4.0E-06; 6.0E-05 55
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 19
rs1129844
CCL11
0.752 0.320 17 34285875 missense variant G/A;C;T snv 0.16; 1.2E-05 13
rs3939286 0.776 0.360 9 6210099 regulatory region variant T/A;C snv 12
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 10
rs1050152
SLC22A4 ; MIR3936HG
0.776 0.480 5 132340627 missense variant C/T snv 0.29 0.28 10
rs34210653
ALOX15
0.807 0.280 17 4632019 missense variant G/A snv 2.7E-02 1.7E-02 8
rs1420101
IL1RL1 ; IL18R1
0.827 0.280 2 102341256 synonymous variant C/T snv 0.33 0.35 8
rs7302200 0.851 0.200 12 56055651 regulatory region variant G/A snv 0.23 6
rs3129878
HLA-DRA
0.807 0.360 6 32440958 intron variant A/C snv 0.30 6
rs1444782 0.851 0.240 10 9016708 intergenic variant G/A snv 0.35 5
rs28383314 0.925 0.160 6 32619436 regulatory region variant T/C snv 0.61 5
rs74767530
CFTR
0.851 0.320 7 117627537 stop gained C/T snv 5.6E-05 4.9E-05 5
rs2428494
HLA-B
0.827 0.160 6 31354420 intron variant T/A;C snv 5
rs9268644
HLA-DRA
0.827 0.360 6 32440267 intron variant A/C snv 0.68 5
rs1888909 0.882 0.200 9 6197392 downstream gene variant T/A;C snv 4
rs10905284
GATA3
0.882 0.200 10 8073399 intron variant C/A;T snv 4
rs8046011 1.000 0.120 16 11226805 downstream gene variant G/A;T snv 3
rs4150407
ERCC3
1.000 0.120 2 127292055 3 prime UTR variant T/C snv 0.47 3
rs4807542
GPX4
1.000 0.120 19 1104079 synonymous variant G/A;C snv 0.22; 1.8E-05 3
rs3807213
IFRD1
0.882 0.200 7 112465699 intron variant G/T snv 0.57 3
rs62408225
BACH2
1.000 0.120 6 90246690 intron variant A/G snv 0.26 2