Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs145204276 0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1057520009 0.790 0.200 2 61492337 missense variant C/T snv 4.4E-06 14
rs5030821
VHL
0.827 0.280 3 10149823 missense variant G/A;C;T snv 4.0E-06 8
rs7664413 0.851 0.160 4 176687553 intron variant C/T snv 0.24 0.25 7
rs80291436
VCX
1.000 0.080 X 7843706 missense variant T/A;C;G snv 4.9E-05; 0.19 3
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1057519747 0.716 0.280 17 7675094 missense variant A/C;G;T snv 23
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1131691021 0.716 0.120 17 7675097 missense variant A/C;G snv 21
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 57
rs121912651 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 53
rs121912664 0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05 44
rs121912665 1.000 0.120 17 7674965 missense variant G/A snv 2.4E-05 7.0E-06 7
rs28934575 0.641 0.400 17 7674230 missense variant C/A;G;T snv 37
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs573154688 1.000 0.160 17 7670711 missense variant C/T snv 4.4E-05 3.5E-05 3
rs730882025 0.724 0.360 17 7674885 missense variant C/A;G;T snv 21
rs762846821 0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs779196500 0.882 0.120 17 7675187 missense variant G/A snv 4.0E-06 5
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs879253942 0.677 0.400 17 7673826 missense variant A/G snv 28
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223