Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
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
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs1143634 0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs397517132 0.623 0.280 7 55191846 missense variant A/T snv 48
rs11571833 0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 43
rs121913355 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 42
rs555607708 0.667 0.360 22 28695869 frameshift variant G/- del 2.0E-03 1.8E-03 33
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
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
rs2735940 0.689 0.400 5 1296371 upstream gene variant A/G snv 0.49 25
rs1535 0.752 0.240 11 61830500 intron variant A/G snv 0.31 24
rs4444235 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 23
rs174537 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 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
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