Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113994136
STAT3
0.827 0.240 17 42329642 missense variant C/A;T snv 7
rs1143679
ITGAM
0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 14
rs114378220
CAMK4
0.851 0.040 5 111230662 intron variant C/T snv 4.5E-02 5
rs114558062 0.851 0.040 3 187923342 intergenic variant T/C snv 6.6E-03 5
rs114846446
LINC01250
0.724 0.240 2 2944140 intron variant G/A snv 9.5E-03 14
rs11571319
CTLA4
2 203874215 downstream gene variant G/A snv 0.17 1
rs11580078
C1orf141 ; IL23R
0.724 0.240 1 67203951 intron variant C/A;G snv 14
rs11586238 0.925 0.160 1 116720516 regulatory region variant C/G snv 0.19 4
rs11594656 0.776 0.240 10 6080046 intergenic variant T/A snv 0.18 9
rs11622435
LOC101928462
0.827 0.120 14 81151652 intron variant G/A snv 4.7E-02 7
rs11675342
TPO
0.851 0.040 2 1403856 intron variant C/T snv 0.40 5
rs11676922
AFF3
0.925 0.160 2 100190478 intron variant T/A snv 0.51 4
rs11711054 1.000 0.080 3 46304120 intergenic variant G/A snv 0.73 2
rs11712165
ARHGAP31
0.882 0.200 3 119399949 intron variant T/G snv 0.30 5
rs117372389
NKD1
0.724 0.240 16 50634166 3 prime UTR variant G/T snv 1.1E-02 14
rs11741255
IRF1-AS1
0.724 0.240 5 132475490 intron variant G/A snv 0.29 14
rs11746555
SLC22A5
0.882 5 132391341 intron variant G/A snv 0.28 4
rs11757201 0.851 0.040 6 137682685 intron variant G/C;T snv 5
rs11785816
LINC00824
0.882 8 128518940 intron variant C/A;G snv 4
rs11805303
C1orf141 ; IL23R
0.827 0.240 1 67209833 intron variant C/T snv 0.30 6
rs11839053 0.724 0.240 13 106410694 intergenic variant T/C snv 7.0E-02 14
rs1190356035
GAD1
0.882 0.360 2 170853979 missense variant G/A snv 7.0E-06 4
rs1194849
SPRED2
2 65379519 intron variant T/C snv 0.49 2
rs11984075
ELMO1
7 37397251 intron variant A/G snv 0.14 2
rs1199047
CCDC88B
0.882 11 64350711 intron variant A/C snv 0.38 4