Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs201943194
DNAH11
0.683 0.480 7 21710596 stop gained C/T snv 8.5E-05 8.4E-05 38
rs1800925
IL13 ; TH2LCRR
0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs153109
IL27
0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs3804100
TLR2
0.633 0.720 4 153704257 synonymous variant T/C snv 9.0E-02 6.7E-02 36
rs1927911
TLR4
0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs2070874
IL4
0.672 0.560 5 132674018 5 prime UTR variant C/T snv 0.28 0.28 27
rs5743618
TLR1
0.677 0.360 4 38797027 missense variant C/A snv 0.53 0.51 25
rs3135932
IL10RA
0.677 0.480 11 117993348 missense variant A/G snv 0.13 0.11 23
rs1805015
IL4R
0.683 0.520 16 27362859 missense variant T/C snv 0.16 0.22 22
rs17855750
IL27
0.695 0.480 16 28503907 missense variant A/C;T snv 6.4E-02; 4.0E-06 21
rs555743307
IL4R
0.695 0.440 16 27342243 missense variant G/A;T snv 3.6E-05; 2.9E-04 20
rs7517847
IL23R ; C1orf141
0.689 0.600 1 67215986 intron variant T/G snv 0.37 19
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs3819024
IL17A
0.701 0.560 6 52185988 upstream gene variant A/G snv 0.34 17
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 16
rs10767664
BDNF
0.752 0.400 11 27704439 intron variant T/A snv 0.83 16
rs2232365
FOXP3
0.716 0.480 X 49259429 intron variant T/C snv 16
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 14
rs721917
SFTPD
0.752 0.360 10 79946568 missense variant A/G snv 0.47 0.42 14
rs7528684
FCRL3
0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 13
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 12
rs4143094
GATA3
0.752 0.240 10 8047173 intron variant T/G snv 0.70 12
rs2227284
IL4
0.732 0.480 5 132677033 intron variant T/C;G snv 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