Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12785878 0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs6918698 0.851 0.200 6 131952117 intron variant G/A;C snv 5
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs9651118 0.683 0.480 1 11802157 intron variant T/C snv 0.18 20
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1799853 0.763 0.320 10 94942290 missense variant C/T snv 9.2E-02 8.9E-02 11
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1801278 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 38
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1805097 0.689 0.360 13 109782884 missense variant C/G;T snv 0.35 22
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs2236225 0.614 0.640 14 64442127 missense variant G/A snv 0.44 0.38 52
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs3730089 0.827 0.280 5 68292320 missense variant G/A snv 0.18 0.22 5
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223