Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6059655 0.790 0.080 20 34077942 intron variant A/G snv 0.95 10
rs470558 1.000 0.040 11 102795585 synonymous variant T/C snv 0.92 0.95 1
rs7297245
HAL
0.882 0.040 12 95980836 missense variant C/T snv 0.85 0.86 4
rs344781 0.807 0.200 19 43670636 upstream gene variant C/T snv 0.80 7
rs7335046 0.807 0.040 13 99389484 downstream gene variant G/C snv 0.80 7
rs8305 0.882 0.120 18 54294435 missense variant G/A snv 0.72 0.78 4
rs751402 0.724 0.360 13 102845848 5 prime UTR variant A/G snv 0.76 15
rs646776 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 25
rs6743068 1.000 0.040 2 201289197 intron variant A/G snv 0.72 1
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs26279 0.790 0.160 5 80873118 missense variant G/A snv 0.73 0.70 9
rs1078305
GSN
1.000 0.040 9 121289122 intron variant A/G snv 0.70 1
rs1340420 0.925 0.080 10 91857549 intron variant A/G snv 0.71 0.70 3
rs1607237 1.000 0.040 3 179232509 intron variant C/T snv 0.68 1
rs2252070 0.752 0.320 11 102955810 upstream gene variant C/T snv 0.68 13
rs4977756 0.683 0.440 9 22068653 intron variant G/A snv 0.64 24
rs4462560 0.851 0.080 15 75355623 3 prime UTR variant G/C snv 0.64 5
rs3087386 0.790 0.160 2 99439044 missense variant A/G snv 0.58 0.61 8
rs7097008 1.000 0.040 10 67849782 non coding transcript exon variant C/A snv 0.60 1
rs2233679 0.763 0.360 19 9834678 splice region variant C/T snv 0.59 11
rs7309332 1.000 0.040 12 7938243 upstream gene variant T/C snv 0.59 3
rs405509 0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 30
rs1412115 0.925 0.080 10 33799125 regulatory region variant T/C snv 0.58 2
rs3846662 0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58 12