Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72613567 0.742 0.320 4 87310240 splice donor variant -/A delins 0.22 14
rs1682111 0.742 0.240 2 54200842 intron variant A/T snv 0.56 13
rs9514828 0.752 0.440 13 108269025 intron variant C/T snv 0.35 12
rs510432 0.752 0.280 6 106326155 upstream gene variant T/C snv 0.57 11
rs843720 0.752 0.280 2 54283523 intron variant T/G snv 0.52 10
rs548234 0.763 0.360 6 106120159 intron variant C/T snv 0.76 11
rs2229113 0.763 0.360 11 117998955 missense variant A/G snv 0.74 0.74 10
rs1161457931 0.763 0.200 22 37084836 missense variant C/T snv 6.4E-06 9
rs1208663703 0.763 0.200 22 37086414 missense variant T/C snv 5.2E-06 7.0E-06 9
rs430397 0.763 0.240 9 125238840 intron variant C/T snv 9.1E-02 0.11 9
rs17580 0.776 0.160 14 94380925 missense variant T/A snv 2.3E-02 2.9E-02 14
rs236918 0.776 0.160 11 117220893 non coding transcript exon variant G/A;C snv 10
rs4374383 0.776 0.200 2 112013193 intron variant A/G snv 0.58 10
rs7270101 0.776 0.200 20 3213247 intron variant A/C snv 8.7E-02 9.7E-02 10
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 10
rs1041740 0.807 0.320 21 31667849 intron variant C/T snv 0.24 8
rs10053538 0.807 0.160 5 157110499 intron variant C/A;T snv 7
rs2234671 0.807 0.240 2 218164385 missense variant C/G snv 9.1E-02 0.11 7
rs12304647 0.807 0.160 12 53991163 intron variant A/C snv 0.26 6
rs4646437 0.827 0.200 7 99767460 intron variant G/A snv 0.30 8
rs11003123 0.827 0.200 10 52771774 upstream gene variant G/A snv 0.30 6
rs4074 0.827 0.200 4 73870427 intron variant A/G snv 0.46 6
rs1012068 0.827 0.160 22 31869917 intron variant T/G snv 0.37 5
rs1054690270 0.827 0.160 8 144505907 frameshift variant CT/- delins 5
rs143175221 0.827 0.200 6 26092952 missense variant T/C snv 8.4E-04 5.6E-04 5