Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 42
rs780094 0.699 0.286 2 27518370 intron variant T/C snp 0.67 29
rs4420638 0.724 0.321 19 44919689 intergenic variant A/G snp 0.19 25
rs2476601 0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92 22
rs10401969 0.801 0.214 19 19296909 intron variant T/C snp 9.8E-02 20
rs1333049 0.715 0.286 9 22125504 intergenic variant G/C snp 0.41 17
rs9939609
FTO
0.580 0.607 16 53786615 intron variant T/A snp 0.42 17
rs1800562 0.463 0.714 6 26092913 missense variant G/A snp 3.3E-02 3.8E-02 17
rs4506565 0.821 0.143 10 112996282 intron variant A/G,T snp 6.4E-05; 0.32 17
rs562338 0.846 0.143 2 21065449 intergenic variant A/G snp 0.71 16
rs671 0.593 0.464 12 111803962 missense variant G/A snp 1.9E-02 1.3E-02 16
rs1799945 0.475 0.679 6 26090951 missense variant C/G snp 0.11 9.9E-02 12
rs7903146 0.596 0.536 10 112998590 intron variant C/G,T snp 0.26 12
rs855791 0.715 0.393 22 37066896 missense variant A/G,T snp 0.57; 4.0E-06 0.65 12
rs635634 0.923 0.107 9 133279427 intergenic variant T/A,C snp 0.17 11
rs1800961 0.923 0.107 20 44413724 missense variant C/T snp 3.1E-02 2.3E-02 11
rs11066280 0.769 0.214 12 112379979 intron variant T/A snp 1.5E-02 10
rs10455872
LPA
0.707 0.179 6 160589086 intron variant A/G snp 4.4E-02 10
rs2075650 0.699 0.357 19 44892362 intron variant A/G snp 0.13 0.14 10
rs3764261 0.769 0.179 16 56959412 intergenic variant C/A snp 0.31 9
rs7138803 0.923 0.107 12 49853685 intergenic variant G/A,T snp 0.32; 3.2E-05 9
rs10195252 1.000 0.071 2 164656581 intron variant T/C snp 0.47 8
rs10938397 0.846 0.179 4 45180510 intergenic variant A/G snp 0.38 8
rs505922 0.724 0.357 None NA snp 0.37 8
rs2925979 1.000 0.071 16 81501185 intron variant T/A,C snp 0.70 8