Disease: Immune System Diseases
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 20
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 20
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46 19
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 14
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 10
rs6840978
IL21-AS1
0.776 0.160 4 122633552 intron variant C/T snv 0.16 10
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 9
rs1738074
LOC105378083 ; LOC107986664 ; TAGAP
0.790 0.320 6 159044945 5 prime UTR variant T/C snv 0.49 9
rs2298428
YDJC
0.807 0.240 22 21628603 missense variant C/T snv 0.27 0.18 9
rs4819388
ICOSLG
0.790 0.240 21 44227538 3 prime UTR variant T/C snv 9
rs13119723
KIAA1109
0.807 0.280 4 122297158 intron variant A/G snv 0.10 8
rs212388
LOC112267968 ; LOC105378083
0.827 0.240 6 159069404 intron variant C/G;T snv 8
rs13003464
PUS10
0.827 0.200 2 60959694 intron variant A/G snv 0.50 7
rs13151961
KIAA1109
0.827 0.200 4 122194347 intron variant A/G snv 0.11 7
rs17810546
IL12A-AS1
0.827 0.440 3 159947262 intron variant A/G snv 8.2E-02 7
rs3748816
MMEL1
0.827 0.200 1 2595307 missense variant A/G snv 0.41 0.46 7
rs802734 0.827 0.280 6 127957653 intergenic variant A/G;T snv 7
rs10806425
BACH2
0.851 0.280 6 90216893 intron variant C/A snv 0.33 6
rs10903122 0.882 0.200 1 24977085 intergenic variant A/G snv 0.56 5
rs11712165
ARHGAP31
0.882 0.200 3 119399949 intron variant T/G snv 0.30 5
rs1250552
ZMIZ1
0.882 0.200 10 79298270 intron variant A/C;G snv 5