Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7234029
PTPN2
0.807 0.320 18 12877061 intron variant A/G snv 0.27 7
rs10956445
CCDC26
1.000 0.120 8 128775730 intron variant T/C snv 0.20 1
rs2004640
IRF5
0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 26
rs3807306
IRF5
0.776 0.320 7 128940626 intron variant G/A;T snv 8
rs10954213
IRF5
0.752 0.200 7 128949373 3 prime UTR variant G/A snv 0.58 11
rs10988542
FNBP1
0.724 0.240 9 129894985 intron variant G/A;C snv 14
rs11741255
IRF1-AS1
0.724 0.240 5 132475490 intron variant G/A snv 0.29 14
rs953387 1.000 0.120 2 136149600 intergenic variant A/C;T snv 1
rs11145763
CARD9
0.724 0.240 9 136369144 intron variant A/C;G;T snv 14
rs2807264 0.724 0.240 X 136583619 downstream gene variant C/A snv 14
rs12863738 0.724 0.240 X 136949968 intron variant C/T snv 0.16 14
rs7831697 0.724 0.240 8 137124061 regulatory region variant T/A;C;G snv 14
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 10
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 14
rs12002949
LOC102723803
1.000 0.120 9 1469317 intergenic variant G/A snv 0.16 1
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs237025
SUMO4 ; TAB2
0.672 0.360 6 149400554 missense variant G/A snv 0.55 0.57 26
rs5743708
TLR2
0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs17435
MECP2
0.851 0.200 X 154046529 intron variant T/A;C snv 4
rs755374 0.724 0.240 5 159402286 intron variant C/T snv 0.28 14
rs34884278 0.724 0.240 1 172869708 intron variant C/T snv 0.63 14
rs2240337
PADI4
0.925 0.200 1 17347727 intron variant C/T snv 9.5E-02 2
rs7660520 0.724 0.240 4 182824168 upstream gene variant G/A;C snv 14
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 9