Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11727676 0.776 0.080 4 144737912 synonymous variant T/C snv 6.6E-02 6.4E-02 14
rs2070699 0.752 0.080 6 12292539 intron variant G/C;T snv 0.45 14
rs4925386 0.776 0.080 20 62345988 intron variant T/C snv 0.56 14
rs12916300 0.742 0.080 15 28165345 intron variant C/T snv 0.50 13
rs58658771 0.776 0.080 15 32709533 intergenic variant T/A snv 0.20 13
rs7229639 0.763 0.080 18 48924606 intron variant A/G snv 0.87 13
rs10821907 0.776 0.080 10 50888694 upstream gene variant C/T snv 0.20 12
rs4360494 0.776 0.080 1 37990219 upstream gene variant G/C snv 0.45 12
rs6058093 0.776 0.080 20 34625392 intron variant A/C snv 0.55 12
rs6584283 0.776 0.080 10 99530544 intron variant T/C snv 0.56 12
rs6691170 0.776 0.080 1 221872104 intergenic variant G/T snv 0.34 12
rs9470361 0.776 0.080 6 36655602 regulatory region variant G/A;T snv 12
rs11255841 0.776 0.080 10 8697617 intergenic variant T/A snv 0.25 11
rs11874392 0.763 0.080 18 48926786 intron variant A/T snv 0.50 11
rs1412834 0.790 0.080 9 22110132 intron variant T/C snv 0.64 11
rs2179593 0.790 0.080 20 44031646 intron variant C/A snv 0.71 11
rs35107139 0.776 0.080 14 53952388 intron variant A/C;G;T snv 11
rs35446936 0.776 0.080 3 169768720 intron variant G/A snv 0.21 11
rs4813802 0.776 0.080 20 6718948 regulatory region variant T/G snv 0.28 11
rs56848936 0.776 0.080 19 45818249 intron variant A/G snv 1.9E-02 11
rs6063514 0.776 0.080 20 50438781 intergenic variant C/T snv 0.42 11
rs10049390 0.776 0.080 3 133982275 intron variant G/A snv 0.67 10
rs10457678 0.790 0.080 6 138801103 intron variant A/G snv 0.19 10
rs10511330 0.776 0.080 3 114402172 intron variant T/C snv 0.22 10
rs1078643 0.776 0.080 17 10803924 missense variant G/A;C snv 10