Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7581886
NPAS2
0.708 0.320 2 100964784 intron variant C/T snv 0.92 18
rs4459895
LPP
0.827 0.160 3 188236626 intron variant A/C snv 0.88 5
rs1274963
CSRNP1
0.925 0.120 3 39149538 non coding transcript exon variant A/G snv 0.82 2
rs2953196
GRAMD1B
0.925 0.120 11 123497625 intron variant A/G snv 0.81 2
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs4240807 0.851 0.160 16 85951755 downstream gene variant A/C snv 0.76 4
rs6489882
OAS3
0.925 0.120 12 112943571 intron variant G/A snv 0.75 2
rs2305160
NPAS2 ; NPAS2-AS1
0.776 0.200 2 100974842 missense variant A/G snv 0.71 0.75 9
rs210142
GGNBP1 ; BAK1
0.925 0.120 6 33579060 intron variant T/C snv 0.74 3
rs210143
GGNBP1 ; BAK1
0.827 0.160 6 33579153 intron variant T/C snv 0.74 6
rs1494555
IL7R
0.790 0.120 5 35871088 missense variant G/A snv 0.64 0.72 8
rs210134
BAK1 ; GGNBP1
1.000 0.120 6 33572432 intron variant A/G snv 0.72 3
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs9271176 0.925 0.120 6 32610350 intergenic variant A/G snv 0.69 2
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs926070
TSBP1-AS1 ; TSBP1
0.827 0.320 6 32289789 intron variant G/A snv 0.68 5
rs2228226
GLI1 ; ARHGAP9
0.851 0.160 12 57472038 missense variant G/C snv 0.60 0.68 6
rs7176508
DRAIC
0.851 0.280 15 69726651 intron variant A/G snv 0.67 4
rs7941765 0.882 0.160 11 128629105 intron variant T/C snv 0.66 3
rs11637565
DRAIC
0.925 0.120 15 69728186 intron variant G/A snv 0.66 2
rs956572
BCL2
0.742 0.280 18 63153338 intron variant A/G snv 0.65 11
rs3803800
TNFSF13 ; TNFSF12-TNFSF13
0.807 0.240 17 7559652 missense variant A/G snv 0.70 0.64 7
rs2651823
C11orf21 ; TSPAN32
0.925 0.120 11 2300420 intron variant A/G snv 0.63 2
rs1128503
ABCB1
0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs1439112
MGAT5
0.851 0.160 2 134305027 intron variant G/A snv 0.61 4