Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3838646
TTTY14
0.827 0.320 Y 18991182 intron variant CA/- del 8
rs52812045
TTTY14
0.851 0.240 Y 18992540 non coding transcript exon variant G/A snv 7
rs8734
TTTY14
Y 18992540 non coding transcript exon variant G/A snv 1
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs12863738 0.724 0.240 X 136949968 intron variant C/T snv 0.16 14
rs179008
TLR7
0.763 0.360 X 12885540 missense variant A/C;T snv 0.18 0.18 14
rs2807264 0.724 0.240 X 136583619 downstream gene variant C/A snv 14
rs3027898
IRAK1
0.752 0.360 X 154010439 downstream gene variant C/A snv 11
rs2294020
CCDC22
0.763 0.280 X 49246763 missense variant A/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
rs3827440
GPR174 ; LOC107985690
0.851 0.120 X 79171491 missense variant T/A;C snv 5.5E-06; 0.51 6
rs755622
MIF-AS1 ; MIF
0.611 0.720 22 23894205 intron variant G/C snv 0.26 44
rs5844572
MIF ; MIF-AS1
0.752 0.360 22 23893562 intron variant -/ATTC delins 11
rs2298428
YDJC
0.807 0.240 22 21628603 missense variant C/T snv 0.27 0.18 9
rs229541
C1QTNF6
0.807 0.200 22 37195278 intron variant G/A snv 0.49 8
rs5754217
UBE2L3
0.925 0.120 22 21585386 intron variant G/T snv 0.31 7
rs743777
IL2RB
0.827 0.200 22 37155567 intron variant A/G snv 0.36 7
rs5754100
UBE2L3
0.882 22 21561877 intron variant T/C snv 0.18 5
rs4821112
UBE2L3
22 21610472 intron variant G/A snv 0.21 4
rs760361706
PPARA
22 46235326 missense variant G/C snv 4.0E-06 4
rs140490
UBE2L3
1.000 0.080 22 21567397 intron variant G/A;C;T snv 2
rs1483068801
P2RX6
1.000 0.120 22 21025861 missense variant T/C snv 1.1E-05 2
rs2836882 0.724 0.240 21 39094644 intergenic variant G/A snv 0.23 15
rs11203203
UBASH3A
0.807 0.240 21 42416077 intron variant G/A snv 0.28 9