Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs907091
IKZF3
0.851 0.280 17 39765489 3 prime UTR variant C/T snv 0.47 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
rs12946510 0.851 0.160 17 39756124 downstream gene variant C/T snv 0.37 5
rs13238352
TNPO3
0.827 0.240 7 129007888 intron variant C/T snv 9.1E-02 5
rs2856683 0.827 0.320 6 32687441 regulatory region variant T/A;C;G snv 0.25 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
rs6933404 0.925 0.280 6 137638098 intergenic variant T/C snv 0.16 5
rs9268644
HLA-DRA
0.827 0.360 6 32440267 intron variant A/C snv 0.68 5
rs9357152 0.827 0.240 6 32697183 regulatory region variant A/G snv 0.24 5
rs9591325
DLEU1
0.851 0.080 13 50237084 intron variant T/C snv 6.0E-02 5
rs11117432 0.851 0.200 16 85985665 upstream gene variant G/A snv 0.15 4
rs11724804
DGKQ
0.882 0.160 4 971991 intron variant G/A snv 0.43 4
rs12134279 0.925 0.080 1 197812068 regulatory region variant C/T snv 0.17 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
rs2006996 0.882 0.080 9 114830358 regulatory region variant T/C snv 7.2E-02 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
rs231725 0.851 0.240 2 203875952 downstream gene variant G/A snv 0.38 4
rs2838519
GATD3A
0.851 0.280 21 44195140 intron variant G/A;C snv 4
rs2942168
LINC02210-CRHR1 ; LINC02210
0.925 0.120 17 45637484 non coding transcript exon variant G/A;C;T snv 0.14 4