Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs11571833 0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 43
rs10936599 0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 32
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs4246215 0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv 29
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 28
rs2735940 0.689 0.400 5 1296371 upstream gene variant A/G snv 0.49 25
rs3802842 0.695 0.280 11 111300984 intron variant C/A snv 0.71 25
rs4939827 0.708 0.160 18 48927093 intron variant T/A;C snv 25
rs1535 0.752 0.240 11 61830500 intron variant A/G snv 0.31 24
rs174537 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 23
rs4444235 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 23
rs1011970 0.677 0.320 9 22062135 intron variant G/T snv 0.23 22
rs7931342 0.689 0.360 11 69227030 intergenic variant T/G snv 0.58 20
rs11200014 0.695 0.280 10 121575416 intron variant G/A;T snv 0.34 19
rs115707823 0.701 0.320 6 30374976 intergenic variant G/A snv 19
rs597808 0.742 0.200 12 111535554 intron variant A/G snv 0.67 19
rs1057941 0.701 0.280 1 155216951 non coding transcript exon variant G/A;T snv 0.46 18
rs11196172 0.708 0.200 10 112967084 intron variant G/A snv 0.13 18
rs12953717 0.724 0.240 18 48927559 intron variant C/T snv 0.36 18
rs16892766 0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02 18
rs174533 0.763 0.160 11 61781553 intron variant G/A snv 0.37 0.29 18
rs4808075 0.701 0.280 19 17279482 intron variant T/C snv 0.26 18