Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9468 0.882 0.080 17 46024197 3 prime UTR variant T/C snv 0.15 0.14 6
rs943437 1.000 0.040 6 111921050 regulatory region variant A/G snv 0.30 1
rs9347683 0.882 0.120 6 162728023 5 prime UTR variant A/C;G snv 3
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs932546861 1.000 0.040 4 99347032 frameshift variant C/- delins 1
rs9323124 0.925 0.040 14 46996974 non coding transcript exon variant T/A snv 0.23 2
rs9275326 1.000 0.040 6 32698883 intergenic variant C/T snv 9.1E-02 1
rs9268515 1.000 0.040 6 32411518 upstream gene variant G/C snv 0.16 1
rs921420972 1.000 0.040 15 48610824 missense variant T/C snv 2.1E-05 1
rs914722 1.000 0.040 1 54048154 intron variant T/A;C snv 1
rs906807 1.000 0.040 18 9117869 missense variant T/C;G snv 0.80; 4.0E-06 1
rs897984 0.925 0.080 16 30875322 non coding transcript exon variant T/C snv 0.62 0.47 2
rs894278 0.882 0.080 4 89813384 intron variant T/G snv 0.15 4
rs893924483 0.716 0.280 11 27658285 missense variant C/A;T snv 4.0E-06 1.4E-05 23
rs892145 1.000 0.040 19 15475861 missense variant A/T snv 0.36 0.38 2
rs886042808 1.000 0.040 6 41161481 missense variant C/G;T snv 4.0E-06 1
rs885479 0.732 0.280 16 89919746 missense variant G/A snv 0.15 8.3E-02 16
rs879253853 1.000 0.040 15 62013057 frameshift variant -/TCTG ins 1
rs878888 1.000 0.040 17 45835269 3 prime UTR variant A/G snv 0.14 1
rs878887 1.000 0.040 17 45835216 3 prime UTR variant C/T snv 0.14 2
rs878886 0.925 0.080 17 45835124 3 prime UTR variant C/G;T snv 3
rs876658902 0.925 0.040 17 7676182 missense variant C/T snv 3
rs875989836 0.925 0.160 11 6394384 missense variant T/C snv 2
rs870575 1.000 0.040 2 45276121 intron variant G/A;C snv 1
rs869312811 0.925 0.040 15 61947292 frameshift variant G/- delins 2