Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs651821 0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 10
rs762679 8 47972876 missense variant T/A snv 0.87 0.88 4
rs8005100 14 58271048 intron variant A/C;G;T snv 0.69 1
rs8012 19 12899706 3 prime UTR variant A/G snv 0.61 0.64 2
rs1134634 4 15601446 3 prime UTR variant G/C;T snv 0.58; 9.4E-06 2
rs1264423 6 30603694 non coding transcript exon variant T/C snv 0.57 0.60 1
rs855791 0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 17
rs4820268 0.851 0.160 22 37073551 missense variant G/A;C snv 0.53; 4.0E-06 5
rs8887 1.000 0.080 19 4502189 3 prime UTR variant T/C;G snv 0.51; 1.8E-05 6
rs13108419 4 121766083 non coding transcript exon variant A/C;G snv 2.3E-05; 0.42 1
rs56261297 8 143992685 splice region variant C/T snv 0.38 0.45 1
rs2278557 16 30082458 intron variant C/G snv 0.37 0.32 1
rs3811444 1 247876149 missense variant C/T snv 0.31 0.26 12
rs1047891 0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 25
rs2246434 1 158648665 intron variant G/A snv 0.26 0.22 1
rs742320 16 792706 intron variant G/A;C snv 0.25; 5.6E-06 1
rs2942194 8 23566156 missense variant A/G snv 0.25 0.21 3
rs563995 19 43774629 intron variant G/A snv 0.24 0.34 3
rs1501466 11 2299654 synonymous variant A/G snv 0.19 0.22 1
rs2902548 10 102727625 intron variant C/T snv 0.18 0.20 1
rs652888 0.776 0.480 6 31883457 non coding transcript exon variant A/G snv 0.18 0.20 4
rs3130618 0.827 0.360 6 31664357 missense variant C/A;T snv 0.15; 4.0E-06 1
rs2270927 5 76295885 missense variant C/A;G;T snv 0.14; 8.1E-06 1
rs113809617 9 137205865 missense variant C/G snv 0.13 0.12 5
rs6525433 X 70853309 missense variant T/C snv 0.12 0.14 1