Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4646 0.716 0.360 15 51210647 3 prime UTR variant A/C snv 0.67 0.70 16
rs5174 0.776 0.240 1 53247055 missense variant C/T snv 0.29 0.28 10
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs5882 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs2303790 0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 19
rs2526378 0.925 0.120 17 58326988 intron variant A/G snv 0.51 2
rs7044343 0.752 0.520 9 6254208 intron variant C/T snv 0.51 13
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv 20
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs4986938 0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33 35
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1138272 0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42
rs4717806 0.776 0.200 7 73702147 intron variant T/A;C snv 9
rs2227564 0.763 0.320 10 73913343 missense variant T/C snv 0.75 0.81 15
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs2231142 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs1051338 0.807 0.120 10 89247603 missense variant T/G snv 0.32 0.26 7
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs7493 0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 24