Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs1260333 0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58 12
rs1263163 11 116802796 intergenic variant G/A snv 0.10 2
rs1265538677 0.790 0.200 13 46055808 synonymous variant A/G snv 4.0E-06 10
rs1289389 13 98684036 3 prime UTR variant C/T snv 0.18 2
rs12953258 1.000 0.080 17 78360015 5 prime UTR variant T/A;G snv 2
rs13266634 0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 23
rs1337503417 0.790 0.160 17 41612325 missense variant G/T snv 4.0E-06 12
rs137852912 0.776 0.120 1 55057454 missense variant G/A;C;T snv 7.2E-05 10
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 28
rs1430583 4 140565830 intron variant C/T snv 0.20 1
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs1685354 11 74002546 intron variant A/G snv 0.30 1
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs17465637 0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 11
rs1746661 0.925 0.080 1 32869438 intron variant G/A;T snv 3
rs1799883 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
rs1799884
GCK
1.000 0.080 7 44189469 intron variant C/T snv 0.17 6
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800206 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs1800588 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 16
rs1800775 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 18
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101