Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504 0.642 0.393 12 111446804 missense variant T/A,C,G snp 0.67 0.67 22
rs1260326 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 20
rs780094 0.699 0.286 2 27518370 intron variant T/C snp 0.67 20
rs579459 0.784 0.107 9 133278724 regulatory region variant C/T snp 0.20 17
rs780093 0.923 0.071 2 27519736 intron variant T/C snp 0.68 16
rs2075650 0.699 0.357 19 44892362 intron variant A/G snp 0.13 0.14 16
rs657152 0.821 0.214 None NA snp 0.41 15
rs1800562 0.463 0.714 6 26092913 missense variant G/A snp 3.3E-02 3.8E-02 13
rs964184 0.756 0.286 11 116778201 3 prime UTR variant G/C snp 0.83 13
rs651007 0.821 0.143 9 133278431 regulatory region variant T/A,C snp 0.20 12
rs4420638 0.724 0.321 19 44919689 intergenic variant A/G snp 0.19 12
rs3764261 0.769 0.179 16 56959412 intergenic variant C/A snp 0.31 11
rs2266788 0.846 0.286 11 116789970 3 prime UTR variant G/A snp 0.93 11
rs11065987 0.846 0.143 12 111634620 intergenic variant A/G snp 0.29 10
rs630014
ABO
1.000 0.036 9 133274306 intron variant G/A,C snp 0.57 10
rs9939609
FTO
0.580 0.607 16 53786615 intron variant T/A snp 0.42 10
rs1532085 0.923 0.071 15 58391167 intron variant A/G,T snp 0.57 10
rs17696736 0.846 0.214 12 112049014 intron variant A/G snp 0.30 10
rs7775698 1.000 0.071 6 135097497 intron variant C/T snp 4.4E-02; 3.2E-05 9
rs6511720 0.769 0.107 19 11091630 intron variant G/T snp 0.11 9
rs157580 0.846 0.214 19 44892009 intron variant G/A snp 0.69 9
rs405509 0.744 0.286 19 44905579 intergenic variant T/G snp 0.58 8
rs646776 0.801 0.214 1 109275908 regulatory region variant C/T snp 0.75 8
rs1864163 0.846 0.107 16 56963321 intron variant G/A snp 0.25 8
rs174547 0.846 0.071 11 61803311 intron variant T/C snp 0.30 8