Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10069690 0.595 0.560 5 1279675 intron variant C/T snv 0.36 19
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 15
rs11571833 0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 21
rs3803662 0.662 0.440 16 52552429 non coding transcript exon variant A/G snv 0.63 3
rs555607708 0.667 0.360 22 28695869 frameshift variant G/- del 2.0E-03 1.8E-03 33
rs1011970 0.677 0.320 9 22062135 intron variant G/T snv 0.23 18
rs2981582 0.695 0.360 10 121592803 intron variant A/G snv 0.58 3
rs4808075 0.701 0.280 19 17279482 intron variant T/C snv 0.26 18
rs2046210 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 6
rs4245739 0.708 0.360 1 204549714 3 prime UTR variant C/A;G snv 0.77; 6.2E-06 6
rs1219648 0.716 0.320 10 121586676 intron variant A/G;T snv 3
rs13281615 0.716 0.360 8 127343372 intron variant A/G snv 0.43 3
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 7
rs41293497 0.724 0.440 13 32340037 stop gained C/A;G;T snv 4.0E-06; 2.0E-05 14
rs8170 0.724 0.160 19 17278895 synonymous variant G/A snv 0.15 0.18 5
rs13387042 0.732 0.280 2 217041109 intergenic variant A/G snv 0.44 3
rs28897672 0.732 0.280 17 43106487 missense variant A/C;G;T snv 3.2E-05 10
rs889312 0.732 0.360 5 56736057 regulatory region variant C/A snv 0.69 3
rs80356898 0.752 0.200 17 43093844 stop gained G/A;C snv 2.8E-05; 4.0E-06 9
rs10941679 0.763 0.120 5 44706396 intergenic variant A/G snv 0.25 2
rs7904519 0.763 0.240 10 113014168 intron variant A/G snv 0.55 3
rs2981579 0.776 0.280 10 121577821 intron variant A/G snv 0.53 4
rs999737 0.776 0.200 14 68567965 intron variant C/T snv 0.16 3
rs137853007 0.790 0.240 22 28725254 missense variant G/A;T snv 5.2E-05 8
rs180177132 0.790 0.280 16 23621362 stop gained C/T snv 6.0E-05 2.1E-05 8