Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3093457
IL9R
1.000 0.120 Y 57184462 intron variant T/G snv 1
rs2232365
FOXP3
0.716 0.480 X 49259429 intron variant T/C snv 16
rs179008
TLR7
0.763 0.360 X 12885540 missense variant A/C;T snv 0.18 0.18 14
rs3027898
IRAK1
0.752 0.360 X 154010439 downstream gene variant C/A snv 11
rs3853839
TLR7
0.752 0.480 X 12889539 3 prime UTR variant C/G;T snv 10
rs1059702
IRAK1
0.807 0.280 X 154018741 missense variant A/G snv 0.72 7
rs1059703
IRAK1
0.851 0.280 X 154013378 missense variant G/A snv 0.67 6
rs371045754
F9
0.882 0.200 X 139530726 upstream gene variant A/C snv 5.5E-06 1.9E-05 4
rs13397
MIR3202-2 ; TMEM187
0.925 0.200 X 153982797 synonymous variant G/A snv 0.27 0.15 2
rs141561256
LOC105373204
1.000 0.120 X 51367945 intron variant G/A snv 4.6E-03 1
rs5917925 1.000 0.120 X 40046169 downstream gene variant G/T snv 0.42 1
rs5987194
MECP2
1.000 0.120 X 154036016 intron variant C/G snv 1
rs6520278
SYN1
1.000 0.120 X 47588525 intron variant C/T snv 0.35 1
rs751650405
NHS
1.000 0.120 X 17719360 missense variant C/G;T snv 3.5E-05 2.9E-05 1
rs755622
MIF-AS1 ; MIF
0.611 0.720 22 23894205 intron variant G/C snv 0.26 44
rs2298383
ADORA2A-AS1 ; ADORA2A ; SPECC1L-ADORA2A
0.827 0.200 22 24429543 non coding transcript exon variant C/A;T snv 11
rs5844572
MIF ; MIF-AS1
0.752 0.360 22 23893562 intron variant -/ATTC delins 11
rs61756766
TNFRSF13C
0.776 0.320 22 41925447 missense variant G/A snv 5.7E-03 5.7E-03 9
rs743777
IL2RB
0.827 0.200 22 37155567 intron variant A/G snv 0.36 7
rs12537
MTMR3 ; HORMAD2-AS1
0.827 0.280 22 30027471 3 prime UTR variant C/T snv 0.40 5
rs2281089
IL2RB
0.851 0.200 22 37136132 intron variant A/G snv 0.17 4
rs4821124 0.851 0.240 22 21625000 downstream gene variant T/C snv 0.19 4
rs5754467
CCDC116 ; YDJC
0.851 0.160 22 21630805 upstream gene variant A/G;T snv 4
rs2283790
UBE2L3
0.882 0.120 22 21602364 intron variant A/G snv 0.21 3
rs11089637 1.000 0.120 22 21624807 downstream gene variant T/C snv 0.28 2