Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 30
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 26
rs13107325 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 24
rs597808 0.742 0.200 12 111535554 intron variant A/G snv 0.67 19
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 18
rs11727676 0.776 0.080 4 144737912 synonymous variant T/C snv 6.6E-02 6.4E-02 14
rs143384 0.827 0.200 20 35437976 5 prime UTR variant G/A snv 0.44 13
rs2075650 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 12
rs998584 6 43790159 downstream gene variant C/A snv 0.41 10
rs2277339 12 56752285 missense variant T/G snv 0.12 0.14 10
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 9
rs459193 0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 9
rs2925979 1.000 0.080 16 81501185 intron variant T/A;C snv 9
rs1128249 1.000 0.080 2 164672114 intron variant G/C;T snv 9
rs1800437 0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 9
rs2074356 0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 9
rs2820443 0.882 0.120 1 219580167 regulatory region variant T/C snv 0.23 8
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 8
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 8
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 8
rs112875651 8 125494452 intron variant G/A snv 0.31 7
rs17451107 3 157079820 upstream gene variant T/C snv 0.38 7
rs2145272 20 6645571 intergenic variant G/A;T snv 7
rs12454712 0.925 0.120 18 63178651 intron variant T/A;C snv 7
rs7607980 1.000 0.080 2 164694691 missense variant T/C snv 0.11 0.13 7