Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10190052 1.000 0.080 2 646674 intergenic variant T/C snv 0.82 1
rs10229583 1.000 0.080 7 127606849 downstream gene variant G/A snv 0.23 1
rs10258074 1.000 0.080 7 15024591 intergenic variant A/T snv 0.54 1
rs10487796 1.000 0.080 7 15023805 intergenic variant T/A snv 0.40 1
rs10490072 1.000 0.080 2 60442796 upstream gene variant T/C snv 0.19 1
rs10738760 0.807 0.320 9 2691186 regulatory region variant A/G snv 0.56 1
rs10757282 1.000 0.080 9 22133985 intergenic variant T/C snv 0.38 1
rs10882102 1.000 0.080 10 92706738 downstream gene variant G/A;C snv 1
rs10906111 1.000 0.080 10 12260358 intergenic variant C/A;G;T snv 1
rs10906115 1.000 0.080 10 12272998 intergenic variant A/G snv 0.37 1
rs10937273 0.882 0.160 3 186831906 downstream gene variant G/A snv 0.33 1
rs10965243 1.000 0.080 9 22130066 downstream gene variant A/G snv 0.13 1
rs10965250 1.000 0.080 9 22133285 intergenic variant G/A snv 0.14 1
rs11036627 1.000 0.080 11 41903164 intergenic variant C/A;T snv 1
rs11634397 1.000 0.080 15 80139880 downstream gene variant A/G snv 0.57 1
rs11873305 1.000 0.080 18 60381959 intron variant A/C snv 0.12 1
rs11927173 1.000 0.080 3 23183703 TF binding site variant T/C snv 0.13 1
rs12143842 0.925 0.160 1 162064100 intergenic variant C/T snv 0.22 1
rs12325830 1.000 0.080 17 56632283 intergenic variant C/T snv 0.46 1
rs12625067 1.000 0.080 20 44315384 upstream gene variant C/A;T snv 1
rs12696304 0.776 0.320 3 169763483 downstream gene variant C/G snv 0.38 1
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 1
rs13081389 1.000 0.080 3 12248301 intergenic variant A/G snv 4.9E-02 1
rs13292136 1.000 0.080 9 79337213 intergenic variant C/G;T snv 1
rs13314285 1.000 0.080 3 23171084 intergenic variant C/A;T snv 1