Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10019888 4 26061368 regulatory region variant A/G snv 0.17 2
rs1011731 1 172377408 intron variant G/A snv 0.46 1
rs10195252 0.925 0.080 2 164656581 intron variant T/C snv 0.48 3
rs1020731 1.000 0.080 2 160287544 intron variant G/A snv 0.69 1
rs1034207 6 127016554 intron variant C/A;G;T snv 0.94 1
rs1051921 0.925 0.120 7 73593613 3 prime UTR variant G/A snv 0.15 6
rs1055144 1.000 0.040 7 25831489 non coding transcript exon variant C/T snv 0.16 2
rs10808546 8 125483576 intron variant C/T snv 0.39 4
rs10894604 11 132771851 non coding transcript exon variant T/G snv 0.26 1
rs11075985
FTO
1.000 0.080 16 53771295 intron variant C/A snv 0.42 2
rs11102800 1.000 0.040 1 114498310 intron variant C/T snv 0.58 1
rs11154370 6 126846446 intron variant A/G;T snv 1
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 9
rs1128249 1.000 0.080 2 164672114 intron variant G/C;T snv 1
rs11724804 0.882 0.160 4 971991 intron variant G/A snv 0.43 1
rs11897119 2 66544868 intron variant T/A;C snv 1
rs12061508 1.000 0.040 1 196615338 intergenic variant G/A snv 0.23 2
rs12110693 6 121837124 intergenic variant G/A snv 0.23 1
rs12440667 1.000 0.040 15 73939098 intron variant C/A;T snv 1
rs12440695 15 62142957 regulatory region variant T/C snv 0.32 2
rs12454712 0.925 0.120 18 63178651 intron variant T/A;C snv 1
rs1254319 1.000 14 60437039 missense variant G/A snv 0.35 0.36 1
rs12714415 2 651430 intergenic variant T/C snv 0.19 2
rs12731740 1 207851475 intron variant C/T snv 9.1E-02 1
rs12936587 0.882 0.080 17 17640408 regulatory region variant G/A snv 0.38 3