Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs629301 0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 19
rs6533530 0.851 0.120 4 110810780 intergenic variant T/C snv 0.47 16
rs6759518 0.851 0.120 2 27263727 intron variant G/C snv 5.5E-02 16
rs7115242 0.851 0.120 11 117037567 intron variant A/G;T snv 16
rs7190256 0.851 0.120 16 72963084 intron variant C/T snv 0.94 16
rs760762 0.851 0.120 20 41147406 intron variant C/A;T snv 0.59 16
rs7632505 0.827 0.120 3 123019460 intron variant A/G snv 0.34 16
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 17
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 17
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs79105258 12 111280427 intron variant C/A;T snv 23
rs799165 0.851 0.120 7 73637727 intergenic variant T/A snv 0.13 16
rs8082812 0.851 0.120 18 8522684 intergenic variant C/A snv 4.6E-02 16
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 35
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 18
rs9942416 5 75741470 intergenic variant C/G snv 0.53 9