Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs187238
IL18
0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs920778
HOTAIR
0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs12212067
FOXO3
0.716 0.320 6 108659993 intron variant T/G snv 0.14 20
rs2424913
DNMT3B
0.708 0.440 20 32786453 intron variant C/T snv 0.56 0.53 18
rs2494938
LRFN2
0.752 0.240 6 40568389 intron variant G/A snv 0.51 11
rs6898743
GHR
0.776 0.160 5 42602390 intron variant C/G snv 0.78 9
rs4767364
NAA25
0.807 0.160 12 112083644 intron variant G/A snv 0.45 8
rs2285947
DNAH11
0.807 0.120 7 21544470 intron variant G/A snv 0.44 7
rs2014300
RUNX1
0.851 0.080 21 34985564 intron variant A/G;T snv 0.75 5
rs10950641
SNX8
0.925 0.040 7 2294751 intron variant G/A snv 2.9E-02 4
rs11016879
MGMT
0.882 0.040 10 129691518 intron variant A/C;G snv 0.66 4
rs4775319
RORA
0.925 0.040 15 60921365 intron variant G/A snv 0.62 4
rs6796803 0.925 0.040 3 186746318 intron variant T/A;C snv 4
rs11752942
LINC00951 ; TDRG1
0.882 0.080 6 40354019 intron variant A/G snv 0.46 3
rs4804217
PCP2
1.000 0.040 19 7634461 intron variant C/T snv 0.29 3
rs522962
PTGIS
0.925 0.040 20 49526825 intron variant T/C snv 0.61 2
rs6019902
PTGIS
0.925 0.040 20 49561676 intron variant G/A snv 0.21 2
rs6125671
PTGIS
0.925 0.040 20 49559061 intron variant C/T snv 0.24 2
rs6598072
SIRT3
0.925 0.040 11 219793 intron variant C/T snv 0.79 2
rs7802034
XRCC2
0.925 0.040 7 152655183 intron variant A/C;G snv 2
rs927068
PTGIS
0.925 0.040 20 49561437 intron variant G/T snv 0.32 2
rs10484761 0.807 0.080 6 40834522 intergenic variant T/C snv 0.31 7