Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 21
rs698 0.724 0.240 4 99339632 missense variant T/A;C snv 0.35 20
rs13212041 0.851 0.200 6 77461407 downstream gene variant C/T snv 0.70 6
rs7958822 0.807 0.200 12 27348173 intron variant G/A snv 0.43 6
rs1034936 0.882 0.080 12 2551994 intron variant C/T snv 0.61 3
rs6350 0.882 0.080 5 1443084 missense variant G/A;C snv 5.6E-02; 6.8E-05 3
rs2567608 0.925 0.080 20 23036445 missense variant T/A;C snv 2.8E-05; 0.49 2