Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs13266634 0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 23
rs4506565 0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs560887 0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 18
rs2657879 1.000 0.080 12 56471554 missense variant A/G snv 0.17 0.15 9
rs17168486 1.000 0.080 7 14858657 intron variant C/T snv 0.18 5
rs6975024
GCK
7 44192287 intron variant T/C snv 0.14 4
rs2232326 2 168907981 missense variant T/C snv 5.1E-03 3.3E-03 3