Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17158930 0.851 0.040 7 111871082 intron variant A/G snv 0.25 4
rs77826363 0.882 0.040 6 1128802 intergenic variant G/T snv 2.2E-02 3
rs1176744 0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 19
rs139459337 0.882 0.040 3 114997018 intron variant C/T snv 4.7E-02 3
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs334558 0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51 20
rs2230912 0.752 0.280 12 121184393 missense variant A/G snv 0.13 0.12 16
rs10494251 0.851 0.040 1 147552120 intron variant C/T snv 5.8E-02 4
rs1541187 0.882 0.040 1 147579693 intron variant C/G;T snv 3
rs672607 0.851 0.040 1 147581540 intron variant G/A snv 0.12 4
rs688325 0.851 0.040 1 147605490 intron variant G/A snv 0.19 4
rs946903 0.882 0.040 1 147625465 3 prime UTR variant T/C snv 0.25 3
rs9364726 0.882 0.040 6 164236705 intergenic variant A/G snv 6.5E-02 3
rs1344706 0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs12476147 0.851 0.040 2 184936178 missense variant A/T snv 0.66 0.59 4
rs11829119 0.851 0.040 12 19040597 intergenic variant T/A;C snv 4
rs10405744 0.851 0.040 19 19948684 intron variant G/A snv 9.0E-02 4
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs165599 0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs231779 0.827 0.160 2 203869764 intron variant C/T snv 0.41 5
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs821616 0.752 0.200 1 232008852 missense variant A/T snv 0.26 0.29 13
rs140504 0.882 0.040 22 23285182 missense variant A/G snv 0.81 0.86 3
rs6586354 0.851 0.040 1 234897489 intron variant G/A snv 0.25 4