Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12201676 0.925 0.040 6 89022382 regulatory region variant T/C snv 0.21 4
rs135745 0.763 0.200 22 38287631 downstream gene variant G/C snv 0.48 13
rs17693963 0.882 0.040 6 27742386 upstream gene variant A/C;G snv 5
rs17746001 0.925 0.040 4 179734472 intergenic variant C/T snv 5.3E-02 4
rs35753505 0.827 0.080 8 31616625 intergenic variant T/A;C snv 6
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 7
rs778293 0.807 0.120 13 105516850 intergenic variant C/A;T snv 7
rs9834970 0.790 0.080 3 36814539 downstream gene variant T/C snv 0.45 9
rs1130214 0.742 0.280 14 104793397 5 prime UTR variant C/A snv 0.31 12
rs3730358 0.724 0.360 14 104780070 intron variant G/A;C snv 0.16; 4.0E-03 14
rs10994359 0.827 0.040 10 60462349 intron variant T/C snv 8.0E-02 7
rs165599 0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs4765905 0.827 0.040 12 2240418 intron variant G/A;C snv 6
rs6484218 0.882 0.040 11 10369034 intron variant G/A snv 0.21 5
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs802568 0.925 0.040 7 146262151 intron variant T/G snv 0.17 4
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs2391191 0.807 0.080 13 105467097 missense variant G/A snv 0.40 0.32 7
rs947267 0.882 0.040 13 105487313 intron variant T/G snv 0.51 4
rs778294 0.851 0.040 13 105489886 synonymous variant C/A;T snv 0.27; 4.0E-06 0.26 5
rs1801028 0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02 24
rs6280 0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57