Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs114002231 1.000 0.080 6 31459618 intron variant G/C snv 1
rs114393147 1.000 0.080 6 33157965 downstream gene variant A/G snv 1
rs114601353 1.000 0.080 6 30389517 intergenic variant C/T snv 1
rs114828403 1.000 0.080 6 32809144 downstream gene variant T/C snv 1
rs115100928 1.000 0.080 6 32419655 intergenic variant G/A snv 1
rs115613607 1.000 0.080 6 32413503 regulatory region variant G/C snv 1
rs115819854 1.000 0.080 6 32683864 intergenic variant G/T snv 1
rs115870917 1.000 0.080 6 29639324 upstream gene variant T/C snv 1
rs116260619 1.000 0.080 6 30479897 intergenic variant A/C snv 1
rs116298963 1.000 0.080 6 32911694 intergenic variant A/G snv 1
rs116381494 1.000 0.080 6 28900717 downstream gene variant C/G snv 1
rs116442863 1.000 0.080 6 29122234 upstream gene variant G/A snv 1
rs116668069 1.000 0.080 6 28800336 intergenic variant C/A;G snv 1
rs116718137 1.000 0.080 6 31228777 upstream gene variant T/C snv 1
rs116718336 1.000 0.080 6 33056722 regulatory region variant G/A snv 1
rs116826541 1.000 0.080 6 29180617 upstream gene variant A/G snv 1
rs11780471 1.000 0.080 8 27487202 upstream gene variant G/A snv 4.3E-02 1
rs12964604 1.000 0.080 18 53635205 intergenic variant C/G;T snv 1
rs13199649 1.000 0.080 6 27901014 upstream gene variant C/T snv 5.0E-02 1
rs13217620 1.000 0.080 6 27685341 upstream gene variant C/T snv 4.7E-02 1
rs151124926 1.000 0.080 2 67740157 intergenic variant A/G;T snv 1
rs192597222 1.000 0.080 5 174713048 intergenic variant C/T snv 2.9E-03 1
rs34244947 1.000 0.080 6 26740141 intergenic variant A/G snv 6.6E-02 1
rs34661125 1.000 0.080 6 28314117 downstream gene variant G/A snv 6.4E-02 1
rs35037868 1.000 0.080 6 27791336 intergenic variant G/A;C snv 1