Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs28929474 0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 37
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs1801253 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 34
rs1047891 0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs13107325 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs2004640 0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 26
rs6214 0.672 0.400 12 102399791 3 prime UTR variant C/T snv 0.45 26
rs11556924 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 21
rs143383 0.724 0.320 20 35438203 5 prime UTR variant G/A snv 0.47 17
rs143384 0.827 0.200 20 35437976 5 prime UTR variant G/A snv 0.44 17
rs12740374 0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 16
rs6570507 0.827 0.240 6 142358435 intron variant G/A snv 0.47 13
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 12
rs3918226 0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 12
rs61776719 0.776 0.120 1 37995647 downstream gene variant C/A snv 0.46 11
rs3791679 0.925 0.120 2 55869757 intron variant A/G snv 0.20 11
rs2247056 0.882 0.160 6 31297713 intron variant T/C snv 0.80 11
rs2277339 12 56752285 missense variant T/G snv 0.12 0.14 10
rs314276 0.807 0.280 6 104960124 intron variant A/C snv 0.65 10
rs185819 0.851 0.200 6 32082290 missense variant T/A;C;G snv 8.2E-06; 0.58; 4.1E-06 10