Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs114142645 1.000 0.040 6 31245806 regulatory region variant T/C snv 2
rs114276265 1.000 0.040 6 31219298 upstream gene variant C/T snv 2
rs114291394 1.000 0.040 6 31383745 upstream gene variant A/C snv 2
rs114508985 1.000 0.040 6 32932241 downstream gene variant C/G;T snv 2
rs114830752 1.000 0.040 6 32715035 upstream gene variant C/A snv 2
rs114867672 1.000 0.040 6 30964067 upstream gene variant T/C snv 2
rs114882497 1.000 0.040 6 32423415 intergenic variant T/C snv 2
rs114904464 1.000 0.040 6 31380300 upstream gene variant G/A snv 2
rs1150688 1.000 0.040 6 28195002 intergenic variant T/C snv 0.54 2
rs115136442 1.000 0.040 6 31086734 downstream gene variant C/A snv 2
rs115165987 1.000 0.040 6 32239404 intergenic variant G/A snv 2
rs115329265 1.000 0.040 6 28744470 intergenic variant A/G;T snv 2
rs115569272 1.000 0.040 6 32995105 intergenic variant G/A snv 2
rs115682897 1.000 0.040 6 32725517 intergenic variant G/A snv 2
rs115687605 1.000 0.040 6 30397852 regulatory region variant C/T snv 2
rs116047537 1.000 0.040 6 32413695 TF binding site variant T/C snv 2
rs116067082 1.000 0.040 6 31222761 upstream gene variant G/A snv 2
rs116137698 1.000 0.040 6 28699892 intergenic variant A/G snv 2
rs116182620 1.000 0.040 6 32511744 intergenic variant A/G snv 5.8E-02 2
rs116326873 1.000 0.040 6 29842049 intergenic variant A/C;G;T snv 2
rs11641947 1.000 0.040 16 58636004 regulatory region variant A/G snv 0.23 2
rs116460775 1.000 0.040 6 32243308 intergenic variant T/C;G snv 2
rs116633139 1.000 0.040 6 32700133 intergenic variant G/A snv 2
rs11787216 1.000 0.040 8 141605122 intron variant C/T snv 0.26 2
rs12522290 1.000 0.040 5 153418096 regulatory region variant C/G snv 0.12 2