Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs12216125 0.925 0.120 6 25997230 intron variant C/T snv 0.26 6
rs3887266 0.925 0.120 6 25843518 intron variant C/T snv 8.9E-02 6
rs1150660 0.925 0.120 6 26101212 upstream gene variant A/C snv 0.73 5
rs115810 0.925 0.120 6 25975655 intron variant G/A;C snv 5
rs129129 0.925 0.120 6 25960801 upstream gene variant A/G snv 0.73 5
rs1540276 0.925 0.120 6 26028591 upstream gene variant T/A;G snv 5
rs198853 0.925 0.120 6 26103868 upstream gene variant T/C snv 0.28 5
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
rs2032447 0.925 0.120 6 26044141 non coding transcript exon variant A/G snv 4.1E-06; 0.67 0.67 5
rs2794719 0.925 0.120 6 26088662 intron variant T/C;G 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
rs4401650 0.925 0.120 6 26034980 upstream gene variant G/A snv 0.75 5
rs442601 0.925 0.120 6 25934296 upstream gene variant G/A snv 0.72 5
rs4766578 0.851 0.200 12 111466567 intron variant T/A snv 0.66 5
rs7756117 0.882 0.160 6 26046337 upstream gene variant G/A snv 0.69 5