Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 64
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 34
rs13107325 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 30
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 29
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 27
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 25
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 16
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 16
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 13
rs3782886 0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 11
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 8
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 7
rs9282858 0.716 0.320 2 31580756 missense variant C/T snv 1.8E-02 2.1E-02 7
rs1800973
LYZ
0.827 0.320 12 69350234 missense variant C/A snv 4.2E-02 4.3E-02 6
rs10392 0.882 0.160 20 38922292 3 prime UTR variant G/A snv 0.17 6
rs147247472 0.925 0.080 1 49441901 intron variant G/A snv 7.3E-04 5
rs2133896 0.925 0.080 12 99455122 intron variant G/T snv 7.6E-02 5
rs11066001 0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 5
rs10196867 0.925 0.080 2 79751234 intron variant C/G;T snv 5
rs10198241 0.925 0.080 2 226115660 intergenic variant T/C snv 0.58 4
rs115357105 0.925 0.080 9 104376689 intergenic variant A/G snv 1.5E-02 4
rs12180309 0.925 0.080 6 91209048 intergenic variant C/T snv 1.9E-02 4
rs55702914 0.925 0.080 2 197349672 intergenic variant C/G snv 0.37 4
rs1789882 1.000 0.080 4 99313896 synonymous variant A/G;T snv 0.82 4
rs1789924 0.925 0.160 4 99353129 upstream gene variant C/G;T snv 4