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 61
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs2075650 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 12
rs3087243 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 7
rs1990760 0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 7
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 6
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 5
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 5
rs13266634 0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 5
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 4
rs5167 1.000 0.040 19 44945208 missense variant T/A;G snv 3.6E-05; 0.39 4
rs157580 0.882 0.160 19 44892009 intron variant G/A snv 0.69 4
rs439401 0.851 0.200 19 44911194 non coding transcript exon variant T/C snv 0.68 3
rs7528684 0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 3
rs689 0.776 0.280 11 2160994 splice region variant A/T snv 0.73 0.60 3
rs1701704 0.851 0.200 12 56018703 intron variant T/G snv 0.25 3
rs428595 1.000 0.120 22 21662102 non coding transcript exon variant A/G snv 0.98 3
rs3842727
TH
1.000 0.120 11 2163618 upstream gene variant G/T snv 0.58 3
rs8106922 1.000 0.080 19 44898409 intron variant A/G snv 0.36 3
rs2304256 0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 3
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 2
rs11755527 0.851 0.360 6 90248512 intron variant C/G snv 0.36 2
rs2292239 0.742 0.480 12 56088396 intron variant T/G snv 0.65 2
rs6859 0.827 0.120 19 44878777 3 prime UTR variant A/G snv 0.58 2