Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs579459 0.784 0.107 9 133278724 regulatory region variant C/T snp 0.20 17
rs2075650 0.699 0.357 19 44892362 intron variant A/G snp 0.13 0.14 16
rs657152 0.821 0.214 None NA snp 0.41 15
rs2074356 0.821 0.214 12 112207597 intron variant G/A snp 8.6E-03 11
rs8050136
FTO
0.744 0.321 16 53782363 intron variant C/A snp 0.40 10
rs9939609
FTO
0.580 0.607 16 53786615 intron variant T/A snp 0.42 10
rs687289 0.923 0.143 None NA snp 0.39 9
rs1121980
FTO
0.923 0.107 16 53775335 intron variant G/A,C snp 0.44 8
rs651821 0.878 0.286 11 116791863 5 prime UTR variant C/T snp 0.88 0.89 7
rs662799 0.769 0.321 11 116792991 regulatory region variant G/A snp 0.90 7
rs9940128
FTO
0.923 0.071 16 53766842 intron variant G/A snp 0.42 6
rs9930506
FTO
1.000 0.071 16 53796553 intron variant A/G snp 0.36 5
rs13389219 1.000 0.071 2 164672366 C/T snp 0.46 4
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
rs7193144
FTO
0.923 0.107 16 53776774 intron variant T/C snp 0.40 4
rs10830963 0.846 0.179 11 92975544 intron variant C/G snp 0.24 4
rs965513 0.784 0.107 9 97793827 intergenic variant A/G,T snp 0.72 4
rs10195252 1.000 0.071 2 164656581 intron variant T/C snp 0.47 3
rs8176719 1.000 0.036 9 133257521 frameshift variant T/TC in-del 0.37 0.37 3
rs998584 6 43790159 regulatory region variant C/A snp 0.41 3
rs77641731
ABO
1.000 0.036 9 133257521 missense variant snp 3
rs863002 1 159205130 intron variant C/T snp 0.29 3
rs6795735 0.923 0.107 3 64719689 intron variant C/A,G,T snp 0.54 3