Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 25
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 21
rs597808 0.742 0.200 12 111535554 intron variant A/G snv 0.67 19
rs174533 0.763 0.160 11 61781553 intron variant G/A snv 0.37 0.29 17
rs10936599 0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 15
rs11727676 0.776 0.080 4 144737912 synonymous variant T/C snv 6.6E-02 6.4E-02 14
rs174537 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 14
rs58658771 0.776 0.080 15 32709533 intergenic variant T/A snv 0.20 13
rs10821907 0.776 0.080 10 50888694 upstream gene variant C/T snv 0.20 12
rs9470361 0.776 0.080 6 36655602 regulatory region variant G/A;T snv 12
rs4759277 0.752 0.160 12 57139907 intron variant C/A snv 0.38 12
rs6058093 0.776 0.080 20 34625392 intron variant A/C snv 0.55 12
rs4360494 0.776 0.080 1 37990219 upstream gene variant G/C snv 0.45 12
rs6063514 0.776 0.080 20 50438781 intergenic variant C/T snv 0.42 11
rs35107139 0.776 0.080 14 53952388 intron variant A/C;G;T snv 11
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 11
rs1537372 0.752 0.120 9 22103184 intron variant G/A;T snv 11
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 11
rs2738783 0.763 0.160 20 63677259 intron variant T/G snv 0.85 11
rs11087784 0.776 0.080 20 7760329 intergenic variant A/G snv 0.13 10
rs11190164 0.776 0.080 10 99591947 intergenic variant A/G snv 0.19 10
rs11255841 0.776 0.080 10 8697617 intergenic variant T/A snv 0.25 10
rs11610543 0.776 0.080 12 42740389 intergenic variant A/G;T snv 10
rs116353863 0.776 0.080 6 31042408 regulatory region variant T/C snv 2.2E-02 10
rs12149163 0.776 0.080 16 86305709 upstream gene variant T/C snv 0.49 10