Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs1047891 0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs11066280 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs3782886 0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 22
rs1800961 0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 21
rs17696736 0.827 0.240 12 112049014 intron variant A/G snv 0.30 18
rs198851 6 26104404 downstream gene variant T/A;C;G snv 15
rs2244608 0.882 0.160 12 120979185 intron variant A/G snv 0.29 9
rs11066015 0.925 0.120 12 111730205 intron variant G/A snv 5.9E-03 5
rs62033406
FTO
16 53790314 intron variant A/G snv 0.33 5
rs11940694
KLB
4 39413373 intron variant A/G snv 0.57 3