Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6749371
STAT4
0.925 0.200 2 191037458 intron variant A/T snv 7.3E-02 2
rs10484718
THEMIS
1.000 0.080 6 127859906 intron variant A/T snv 8.6E-02 1
rs58911644
GATD3A ; LOC107983952 ; LOC102725065
1.000 0.080 21 44209238 3 prime UTR variant A/T snv 1
rs859715 1.000 0.080 1 172790982 intron variant A/T snv 0.36 1
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 26
rs35829419
NLRP3
0.689 0.560 1 247425556 missense variant C/A snv 3.9E-02 3.3E-02 23
rs2807264 0.724 0.240 X 136583619 downstream gene variant C/A snv 14
rs1457092
MYO9B
0.790 0.320 19 17193427 intron variant C/A snv 0.44 8
rs10806425
BACH2
0.851 0.280 6 90216893 intron variant C/A snv 0.33 6
rs2816316
LOC105371664
0.882 0.200 1 192567683 intron variant C/A snv 0.79 5
rs2474619
BACH2
0.882 0.360 6 90170316 intron variant C/A snv 0.72 3
rs11217040 0.925 0.200 11 118809939 regulatory region variant C/A snv 0.19 2
rs12727642 1.000 0.080 1 7986612 upstream gene variant C/A snv 0.12 1
rs187238
IL18
0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs62324212
IL21-AS1
0.724 0.240 4 122639784 intron variant C/A;G snv 15
rs11580078
C1orf141 ; IL23R
0.724 0.240 1 67203951 intron variant C/A;G snv 14
rs6032606
ZNF335
1.000 0.080 20 45967568 missense variant C/A;G snv 0.84 1
rs28940580
MEFV
0.742 0.560 16 3243447 missense variant C/A;G;T snv 1.0E-04; 8.0E-06 17
rs76830965
IL12A-AS1
0.925 0.120 3 159919889 intron variant C/A;G;T snv 3
rs1359062
LOC105371664
0.925 0.160 1 192572342 intron variant C/A;G;T snv 2
rs4558075 1.000 0.080 10 6359663 intergenic variant C/A;G;T snv 1
rs971290 1.000 0.080 14 68805252 intergenic variant C/A;G;T snv 1
rs80356624
KCNJ11
0.752 0.240 11 17387490 missense variant C/A;T snv 16
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 9