Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1015164 0.925 3 46410189 intron variant A/C;G;T snv 8
rs10808739 0.882 8 64727703 intron variant G/A snv 0.24 6
rs10892324 0.925 11 119032329 upstream gene variant T/A;G snv 5
rs11231017 0.925 11 62293877 downstream gene variant G/A snv 0.29 5
rs11649112 0.925 16 13267554 intron variant G/A snv 0.22 5
rs12460243 0.925 19 8066356 intron variant G/A snv 0.14 5
rs13064773 0.925 3 158893105 intergenic variant G/A snv 0.39 5
rs16823858 0.925 3 115559835 intron variant G/A;C snv 5
rs16933829 0.925 11 17094129 intron variant T/C snv 6.2E-02 5
rs17038463 0.925 3 1383484 intron variant T/C;G snv 5
rs17151904 0.925 7 25568789 TF binding site variant G/A;C snv 5
rs17169 0.925 2 8037334 intron variant G/T snv 0.13 5
rs17691394 0.925 7 126684537 intron variant A/G snv 0.13 5
rs30388
MAF
0.925 16 79580219 regulatory region variant T/C;G snv 5
rs3869068 0.925 6 30036275 intron variant C/T snv 0.17 5
rs4835796 0.925 5 138446426 3 prime UTR variant T/G snv 0.56 5
rs59440261 0.925 6 31403294 intron variant C/A snv 3.3E-02 5
rs608114 0.925 6 95928822 intron variant A/T snv 0.95 5
rs61550741 0.925 21 31133966 intron variant A/G snv 0.12 5
rs6542826 0.925 2 109433263 intron variant A/G snv 0.51 5
rs6594357 0.925 5 109205522 intergenic variant T/A;C snv 5
rs6723162 0.925 2 70875156 intergenic variant A/T snv 0.65 5
rs7458938 0.925 7 125820594 intergenic variant G/A snv 0.72 5
rs7576600 0.925 2 40840846 intergenic variant C/A;G snv 5
rs183662584 1.000 3 46373218 missense variant G/A snv 5.2E-04 1.5E-04 2