Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4065275
ORMDL3
0.807 0.160 17 39924612 intron variant A/G;T snv 0.56 6
rs6974491
ELMO1
0.807 0.120 7 37334906 intron variant G/A snv 0.14 6
rs10445308
IKZF3
0.851 0.240 17 39781794 intron variant C/T snv 0.38 5
rs12531711
TNPO3
0.827 0.200 7 128977412 intron variant A/C;G snv 5
rs13238352
TNPO3
0.827 0.240 7 129007888 intron variant C/T snv 9.1E-02 5
rs582054
IL12A ; IL12A-AS1
0.882 0.160 3 159992214 intron variant A/C;T snv 5
rs6659932
IL12RB2
0.827 0.240 1 67336688 intron variant A/C snv 0.81 5
rs9268644
HLA-DRA
0.827 0.360 6 32440267 intron variant A/C snv 0.68 5
rs9591325
DLEU1
0.851 0.080 13 50237084 intron variant T/C snv 6.0E-02 5
rs11724804
DGKQ
0.882 0.160 4 971991 intron variant G/A snv 0.43 4
rs1372072
PLCL2
0.851 0.200 3 16913767 intron variant G/A snv 0.35 4
rs17649553
MAPT
0.882 0.160 17 45917282 intron variant C/T snv 0.14 4
rs17690703
MAPT-AS1
0.882 0.160 17 45847931 intron variant C/T snv 0.18 4
rs199505
WNT3 ; LRRC37A2
0.925 0.120 17 46782044 intron variant A/G snv 0.84 4
rs2041670
CLEC16A
0.851 0.280 16 11080795 intron variant G/A;C snv 4
rs2075533
DELEC1 ; TNFSF8
0.851 0.160 9 114931351 intron variant G/A;T snv 4
rs2838519
GATD3A
0.851 0.280 21 44195140 intron variant G/A;C snv 4
rs3790567
IL12RB2
0.851 0.240 1 67356694 intron variant A/G snv 0.61 4
rs492899
CYP21A2 ; SKIV2L
0.882 0.240 6 31965741 intron variant T/C snv 0.12 0.15 4
rs622342
SLC22A1
0.882 0.280 6 160151834 intron variant C/A snv 0.70 4
rs7208487
FBXL20
0.925 0.080 17 39387196 intron variant T/A;G snv 4
rs725613
CLEC16A
0.851 0.240 16 11075826 intron variant T/G snv 0.42 4
rs911263
RAD51B
0.851 0.200 14 68286876 intron variant C/T snv 0.57 4
rs1008723
GSDMB
0.925 0.160 17 39910014 intron variant G/C;T snv 3
rs10174098
ITGAV
0.882 0.200 2 186628015 intron variant G/A snv 0.62 3