Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17445836 0.851 0.320 16 85984057 intron variant G/A snv 0.15 5
rs2269067
C5
0.827 0.360 9 120974762 intron variant G/C snv 0.20 0.30 5
rs3757247
BACH2
0.827 0.320 6 90247744 intron variant C/T snv 0.38 5
rs9266409 0.925 0.200 6 31368791 intron variant T/C snv 0.22 5
rs947474
LINC02649 ; LINC02656
0.827 0.440 10 6348488 intron variant G/A snv 0.79 5
rs10863888
TRAF5
0.851 0.280 1 211329427 intron variant A/C;G;T snv 4
rs12569232
LOC107985258
0.882 0.280 1 211379722 intron variant G/C;T snv 4
rs1310182
AP4B1-AS1 ; PTPN22
0.882 0.360 1 113830881 intron variant A/C;G snv 0.56 4
rs2058660
IL18RAP
0.882 0.280 2 102437989 intron variant G/A snv 0.78 4
rs2838519
GATD3A
0.851 0.280 21 44195140 intron variant G/A;C snv 4
rs573775
ATG5
0.851 0.320 6 106316991 intron variant G/A snv 0.34 4
rs762421
GATD3A
0.851 0.360 21 44195678 intron variant G/A snv 4
rs2253907 0.882 0.360 6 31369093 intron variant C/T snv 0.43 3
rs2474619
BACH2
0.882 0.360 6 90170316 intron variant C/A snv 0.72 3
rs310241
JAK1
0.882 0.360 1 64837655 intron variant A/G snv 0.37 3
rs3790622
IL19 ; IL10
0.882 0.320 1 206771818 intron variant G/A snv 1.5E-03 3
rs4795067
NOS2
0.882 0.280 17 27779649 intron variant A/G snv 0.31 3
rs7753873
LOC107986649 ; WAKMAR2
0.882 0.320 6 137852285 intron variant A/C snv 0.18 3
rs9494885
LOC107986649 ; WAKMAR2
0.882 0.320 6 137851611 intron variant T/C snv 0.20 3
rs10515746
HAVCR2
0.925 0.240 5 157109557 intron variant A/C;T snv 2
rs12212193
BACH2
0.925 0.280 6 90287050 intron variant A/G snv 0.38 2
rs12932187
LOC105371080 ; CIITA
0.925 0.320 16 10878023 intron variant C/G;T snv 2
rs17127024
JAK1
0.925 0.280 1 64837448 intron variant G/T snv 5.1E-02 2
rs2489188
TGFBR3
0.925 0.200 1 91866932 intron variant C/T snv 0.65 2
rs2903908
NCOA5
0.925 0.200 20 46065308 intron variant T/C snv 0.22 2