Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6062302 0.882 0.040 20 63689615 synonymous variant T/C snv 0.74 0.81 4
rs2297440 0.763 0.080 20 63680946 intron variant T/C snv 0.81 10
rs10464870 0.882 0.040 8 129465577 intron variant C/T snv 0.80 3
rs8957 0.925 0.040 20 63742354 missense variant G/T snv 0.71 0.78 2
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs6971 0.742 0.200 22 43162920 missense variant A/G snv 0.76 0.75 11
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs2562152 0.882 0.040 16 73898 intron variant A/T snv 0.67 4
rs7003908 0.716 0.320 8 47858141 intron variant C/A snv 0.66 16
rs4977756 0.683 0.440 9 22068653 intron variant G/A snv 0.64 24
rs1128503 0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs2440472 0.827 0.080 16 56402912 intron variant A/G snv 0.61 5
rs1005230 0.827 0.040 6 43768759 upstream gene variant T/C snv 0.60 5
rs145929329 0.882 0.040 9 22066213 intron variant TTTT/-;T;TT;TTT;TTTTT;TTTTTT;TTTTTTTTTT delins 0.58 3
rs4652 0.752 0.200 14 55138318 missense variant A/C snv 4.1E-06; 0.45 0.57 12
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs723527 0.882 0.040 7 55067179 intron variant A/G snv 0.53 4
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs3788266 0.732 0.160 21 46606442 upstream gene variant G/A snv 0.50 12
rs12230172 0.882 0.040 12 75848895 intron variant A/G snv 0.48 4
rs2235573 0.882 0.040 22 38081923 synonymous variant G/A snv 0.47 0.46 4
rs3829382 0.925 0.040 13 28003551 3 prime UTR variant G/T snv 0.46 2
rs7325927 0.925 0.040 13 107823165 intron variant C/T snv 0.38 2