Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs657152 0.821 0.214 None NA snp 0.41 15
rs687289 0.923 0.143 None NA snp 0.39 9
rs507666 0.846 0.036 None NA snp 0.17 4
rs12075 1.000 0.071 1 159205564 missense variant G/A snp 0.51 0.64 4
rs3027012 1 159204333 5 prime UTR variant C/T snp 0.13 4
rs863002 1 159205130 intron variant C/T snp 0.29 3
rs10747502 1.000 0.036 1 99058491 intron variant A/G snp 0.86 2
rs1011731 1 172377408 intron variant G/A snp 0.47 1
rs1056513 1 61914626 missense variant G/A,C snp 0.57; 8.0E-06 0.50 1
rs12023396 1 231134890 intergenic variant A/G snp 0.21 1
rs2427837 0.923 0.071 1 159288755 intergenic variant G/A snp 0.22 1
rs2820443 1.000 0.071 1 219580167 regulatory region variant T/C snp 0.23 1
rs2820464 1 219519878 intergenic variant G/A,C snp 0.28 1
rs316662 1 84321629 intron variant A/C,T snp 0.88; 1.6E-04 1
rs333960 1 109896858 non coding transcript exon variant C/A,T snp 6.4E-05; 0.77 1
rs4846567 1 219577375 intergenic variant G/T snp 0.22 1
rs6701231 1 118953038 intron variant C/A,G snp 0.33 1
rs863006 1 159207958 non coding transcript exon variant G/A snp 0.54 1
rs984222 1 118961220 intron variant C/A,G snp 0.59 1
rs13389219 1.000 0.071 2 164672366 C/T snp 0.46 4
rs10195252 1.000 0.071 2 164656581 intron variant T/C snp 0.47 3
rs10198552 2 134842306 intron variant T/C snp 6.0E-02 1
rs1020410 2 175919410 intergenic variant T/C snp 0.33 1
rs1128249 1.000 0.071 2 164672114 intron variant G/C,T snp 0.46 1
rs1374313 2 119388079 regulatory region variant T/C snp 0.56 1