Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9923544
FTO
1.000 0.080 16 53768073 intron variant C/T snv 0.42 2
rs1011731 1 172377408 intron variant G/A snv 0.46 1
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
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
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
rs12440667 1.000 0.040 15 73939098 intron variant C/A;T snv 1
rs12454712 0.925 0.120 18 63178651 intron variant T/A;C snv 1
rs12731740 1 207851475 intron variant C/T snv 9.1E-02 1
rs1294410 6 6738519 intron variant T/C snv 0.65 1
rs1406948 20 35317816 intron variant G/A snv 0.44 1
rs17109256 14 79473650 intron variant G/A snv 0.21 1
rs17213965 16 15788110 intron variant C/T snv 0.24 1
rs1993709 1.000 0.080 1 72372846 intron variant A/G snv 0.85 1
rs2235529 1.000 0.040 1 22123994 intron variant C/T snv 0.13 1
rs2894204 1.000 0.040 6 31269284 intron variant C/A;T snv 1
rs3786897 1.000 0.080 19 33402102 intron variant A/G snv 0.45 1
rs4580892 6 127088737 intron variant C/T snv 0.32 1
rs4640244 17 21380911 intron variant A/G snv 0.33 1
rs4686340 3 9303534 intron variant A/C snv 0.80 1
rs55747707 7 73623036 intron variant G/A snv 0.16 1
rs605203 1.000 0.120 6 31879235 intron variant C/A snv 0.77 1