Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
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
rs1805794
NBN
0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 41
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs763059810 0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs937475913 0.790 0.120 8 47936435 missense variant T/C snv 4.0E-06 7
rs153109 0.623 0.600 16 28507775 intron variant T/C snv 0.43 37