Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10930046
IFIH1
0.882 0.200 2 162281473 missense variant T/C snv 9.7E-02 0.16 3
rs13015714
IL18R1
0.882 0.200 2 102355405 intron variant G/T snv 0.77 3
rs6432714
IFIH1
0.882 0.160 2 162280842 intron variant A/T snv 0.16 3
rs6726160
NONOP2
1.000 0.080 2 60937594 non coding transcript exon variant T/G snv 0.47 3
rs10188217
PUS10
0.925 0.080 2 60990407 intron variant T/A;C snv 2
rs10203477
LINC01185
0.925 0.200 2 60877850 intron variant A/T snv 0.48 2
rs11123810
AFF3
0.925 0.200 2 100142823 intron variant T/C snv 0.37 2
rs1468788
SLC9A4
1.000 0.080 2 102476054 intron variant C/T snv 0.54 2
rs16867384
LINC01934
0.925 0.200 2 181246479 intron variant T/C snv 0.19 2
rs6749371
STAT4
0.925 0.200 2 191037458 intron variant A/T snv 7.3E-02 2
rs990171 1.000 0.080 2 102470310 upstream gene variant A/C snv 0.78 2
rs1018326
LINC01934
1.000 0.080 2 181143073 intron variant T/C snv 0.47 1
rs13401064
STAT4
1.000 0.080 2 191105604 intron variant C/G snv 8.5E-02 1
rs45620941
CD28
1.000 0.080 2 203735734 3 prime UTR variant G/T snv 0.14 1
rs62184863 1.000 0.080 2 203819074 intergenic variant G/C snv 6.2E-02 1
rs6715106
STAT4
1.000 0.080 2 191048308 intron variant A/G snv 6.1E-02 1
rs6752770
STAT4
1.000 0.080 2 191108837 intron variant A/G snv 0.31 1
rs10936599
MYNN
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 32
rs4625
DAG1
0.716 0.280 3 49534707 3 prime UTR variant A/G snv 0.30 17
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 9
rs17810546
IL12A-AS1
0.827 0.440 3 159947262 intron variant A/G snv 8.2E-02 7
rs2030519
LPP
0.827 0.200 3 188402113 intron variant G/A snv 0.61 7
rs11712165
ARHGAP31
0.882 0.200 3 119399949 intron variant T/G snv 0.30 5
rs13098911
CCR3
0.882 0.200 3 46193709 intron variant C/G;T snv 5
rs13314993
LOC105377022
0.882 0.200 3 32973977 regulatory region variant G/C;T snv 5