Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs780093 0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs864745 0.763 0.320 7 28140937 intron variant T/C snv 0.41 12
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 17
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1050450 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs17235409 0.653 0.600 2 218395009 missense variant G/A;C snv 4.9E-02; 4.1E-06 31
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs35829419 0.689 0.560 1 247425556 missense variant C/A snv 3.9E-02 3.3E-02 23
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42