Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs199726 0.925 0.120 6 25953132 intergenic variant G/A snv 0.73 5
rs199734 0.925 0.120 6 25940165 intergenic variant G/A;C snv 5
rs199736 0.925 0.120 6 25936559 intergenic variant C/T snv 0.72 5
rs199737 0.925 0.120 6 25933310 upstream gene variant A/C;T snv 5
rs199739 0.925 0.120 6 25960281 upstream gene variant A/C;G snv 0.78 5
rs199751 0.925 0.120 6 26015355 upstream gene variant T/C snv 0.77 5
rs199752 0.925 0.120 6 26012647 upstream gene variant C/T snv 0.77 5
rs199753 0.925 0.120 6 26001660 non coding transcript exon variant G/A snv 0.77 5
rs218264 4 54542708 intergenic variant A/G;T snv 5
rs35385468 0.925 0.120 6 26101212 upstream gene variant -/C delins 9.7E-03 5
rs386406569 0.925 0.120 6 26101212 upstream gene variant -/C delins 5
rs442601 0.925 0.120 6 25934296 upstream gene variant G/A snv 0.72 5
rs4672497 2 62296430 TF binding site variant C/G;T snv 5
rs532398216 16 182398 downstream gene variant TGAG/- delins 2.0E-03 5
rs6014993 20 57416581 regulatory region variant A/G snv 0.58 5
rs632057 6 139512875 intron variant T/G snv 0.57 5
rs634869 6 139510620 intron variant T/A;C snv 5
rs668459 6 139514552 intron variant C/T snv 0.51 5
rs78744187 19 33263642 intergenic variant C/T snv 6.8E-02 5
rs7955734 12 4223993 intergenic variant C/G snv 0.22 5
rs807212 0.925 0.120 6 26065393 regulatory region variant A/G;T snv 5
rs9295684 0.925 0.120 6 26069441 intergenic variant T/C snv 0.38 5
rs9358901 0.925 0.120 6 26024208 downstream gene variant G/T snv 0.67 5
rs9379818 0.925 0.120 6 26022978 downstream gene variant G/A;T snv 5
rs9804550 11 5164863 intergenic variant T/A;C snv 5