Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs12203592
IRF4
0.649 0.320 6 396321 intron variant C/T snv 0.10 38
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20 31
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32 29
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 28
rs895520
NPAS2
0.689 0.320 2 100961475 intron variant G/A snv 0.35 23
rs10165970
NPAS2
0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs10519097
RORA
0.708 0.320 15 60997989 intron variant C/T snv 0.13 18
rs11943456
TMEM165
0.708 0.320 4 55410167 intron variant T/C snv 0.42 18
rs17024869
NPAS2
0.708 0.320 2 100843581 intron variant T/C snv 8.3E-02 18
rs7581886
NPAS2
0.708 0.320 2 100964784 intron variant C/T snv 0.92 18
rs2071286
NOTCH4
0.752 0.280 6 32212119 intron variant C/T snv 0.17 12
rs3131379
MSH5 ; MSH5-SAPCD1
0.752 0.440 6 31753256 intron variant G/A snv 6.4E-02 7.9E-02 10
rs3817198
LSP1
0.790 0.280 11 1887776 intron variant T/C snv 0.26 8
rs41291957
CARMN ; MIR145 ; MIR143
0.882 0.200 5 149428827 intron variant G/A snv 0.12 7
rs6449182
CD38
0.807 0.160 4 15778830 intron variant C/G snv 0.22 6
rs2069812
IL5
0.851 0.240 5 132544224 intron variant A/G snv 0.54 5
rs4833103
TLR1
0.925 0.160 4 38813881 intron variant A/C snv 0.64 5
rs113686495
CASP8
0.925 0.160 2 201258757 intron variant ATTCTGTC/- delins 4
rs3769821
CASP8
0.851 0.200 2 201258707 intron variant C/T snv 0.57 4
rs4150506
ERCC3
0.851 0.120 2 127262970 intron variant G/A snv 0.18 4
rs537160
CYP21A2 ; CFB
0.882 0.240 6 31948623 intron variant A/G snv 0.73 4