Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10798801 1.000 0.080 1 30760633 upstream gene variant A/G snv 0.64 1
rs10892301 1.000 0.080 11 118864767 intergenic variant G/A;T snv 1
rs10903340 1.000 0.080 8 11593078 regulatory region variant T/A;C;G snv 1
rs10911628 1.000 0.080 1 184680369 intergenic variant C/A snv 9.4E-02 1
rs10946940 1.000 0.080 6 27592808 upstream gene variant A/C;G snv 1
rs10947345 1.000 0.080 6 32782018 intergenic variant T/A snv 1
rs11185602 1.000 0.080 7 50259481 intron variant A/G snv 0.34 1
rs11185603 1.000 0.080 7 50267214 upstream gene variant C/A;G snv 0.26 1
rs112047269 1.000 0.080 2 185151747 intergenic variant T/C snv 7.2E-02 1
rs11231824 1.000 0.080 11 64587323 upstream gene variant G/A;C;T snv 1
rs114038709 1.000 0.080 17 45379362 intergenic variant C/T snv 1
rs114090659 1.000 0.080 6 30973212 intergenic variant T/C snv 1
rs114092478 1.000 0.080 6 32714358 upstream gene variant C/T snv 1
rs11644034 1.000 0.080 16 85939006 intron variant G/A snv 0.19 1
rs11655550 1.000 0.080 17 39453870 upstream gene variant T/C snv 0.16 1
rs116727542 1.000 0.080 6 32453450 intergenic variant A/G;T snv 1
rs11697848 1.000 0.080 20 49958778 downstream gene variant C/T snv 3.6E-02 1
rs11724582 1.000 0.080 4 122470309 intergenic variant A/G snv 0.22 1
rs11725913 1.000 0.080 4 121656537 TF binding site variant G/T snv 0.14 1
rs12444486 1.000 0.080 16 85959043 downstream gene variant C/T snv 0.55 1
rs12537284 1.000 0.080 7 129077852 intergenic variant G/A snv 0.11 1
rs12575600 1.000 0.080 11 128454974 downstream gene variant C/G;T snv 1
rs12753920 1.000 0.080 1 92200342 upstream gene variant A/G snv 0.31 1
rs12876893 1.000 0.080 13 30828694 regulatory region variant G/A snv 0.31 1
rs12971295 1.000 0.080 19 18406521 regulatory region variant G/A snv 0.31 1