Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1111875 0.776 0.360 10 92703125 intergenic variant C/T snv 0.36 10
rs6921438 0.776 0.360 6 43957870 intergenic variant G/A;C snv 10
rs10759931 0.790 0.360 9 117701869 upstream gene variant G/A;T snv 9
rs1800592 0.807 0.200 4 140572807 upstream gene variant T/C snv 0.40 8
rs10738760 0.807 0.320 9 2691186 regulatory region variant A/G snv 0.56 7
rs1073203 0.882 0.160 5 125983763 intron variant C/G snv 0.15 4
rs2808629 0.925 0.160 1 159707006 upstream gene variant G/A snv 0.31 3
rs955333 0.882 0.240 6 154626274 intergenic variant A/G snv 0.13 3
rs9896052 0.882 0.160 17 75422781 intergenic variant A/C snv 0.50 3
rs11018670 0.925 0.160 11 89623460 intergenic variant A/G snv 0.30 2
rs12219125 0.925 0.120 10 20304158 intergenic variant G/T snv 0.15 2
rs184340784 0.925 0.160 1 4529823 intergenic variant C/T snv 6.1E-04 2
rs200295620 0.925 0.160 3 168172398 intergenic variant T/-;TT delins 5.7E-03 2
rs4462262 0.925 0.120 10 57429418 intergenic variant T/C snv 0.55 2
rs599019 0.925 0.160 18 294495 intergenic variant C/A snv 0.78 2
rs6427247 0.925 0.160 1 170411339 regulatory region variant A/G snv 0.26 2
rs6704078 0.925 0.200 1 216437370 intergenic variant C/T snv 0.94 2
rs1145612 1.000 0.120 5 158271107 upstream gene variant C/A snv 0.49 1
rs114790220 1.000 0.120 8 5306434 intergenic variant T/A;C snv 1
rs11662496 1.000 0.120 18 43695432 intergenic variant A/G;T snv 1
rs11771617 1.000 0.120 7 125733372 intergenic variant A/G snv 0.20 1
rs13064954 1.000 0.120 3 157136953 downstream gene variant G/A snv 7.9E-02 1
rs17404956 1.000 0.120 5 166962488 regulatory region variant A/G snv 5.5E-02 1
rs2104455 1.000 0.120 6 9368285 intergenic variant A/G snv 0.30 1