Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1047972 0.716 0.240 20 56386407 missense variant T/C snv 0.85 0.84 19
rs13419896 0.776 0.240 2 46329206 intron variant G/A snv 0.10 8
rs1864183 0.742 0.240 5 82253397 missense variant C/T snv 0.52 0.40 12
rs2031920 0.695 0.240 10 133526341 non coding transcript exon variant C/T snv 3.1E-02 20
rs3754093 0.776 0.240 1 241846814 upstream gene variant A/G snv 0.23 11
rs587781991 0.724 0.240 17 7675208 missense variant C/A;T snv 17
rs62514004 0.790 0.240 8 133190246 upstream gene variant A/G snv 0.28 8
rs10012 0.716 0.280 2 38075247 missense variant G/C snv 0.31 0.36 16
rs1047840 0.708 0.280 1 241878999 missense variant G/A snv 0.36 0.40 19
rs132774 0.776 0.280 22 41635949 intron variant C/G snv 0.69 9
rs2073498 0.763 0.280 3 50332115 missense variant C/A snv 9.6E-02 8.0E-02 12
rs2107425 0.732 0.280 11 1999845 intron variant C/T snv 16
rs3734091 0.689 0.280 5 83204915 missense variant G/T snv 2.3E-02 1.4E-02 19
rs7025417 0.752 0.280 9 6240084 intron variant T/C;G snv 11
rs745564626 0.752 0.280 14 103699003 missense variant C/G;T snv 4.3E-05 14
rs132770 0.752 0.320 22 41621260 5 prime UTR variant A/G snv 0.83 14
rs1360485 0.742 0.320 13 30457747 3 prime UTR variant C/T snv 0.58 16
rs145204276 0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31
rs2267437 0.724 0.320 22 41620695 intron variant C/A;G snv 19
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs4796793 0.716 0.320 17 42390192 upstream gene variant G/C snv 0.67 16
rs5751129 0.752 0.320 22 41619761 intron variant C/T snv 0.69 14
rs6505162 0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05 25
rs709816
NBN
0.752 0.320 8 89955483 synonymous variant A/G snv 0.47 0.51 10
rs752742313 0.637 0.320 3 138655502 missense variant C/T snv 1.2E-05 36