Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 106
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 75
rs1800925 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs2853676 0.667 0.560 5 1288432 intron variant T/A;C snv 23
rs2076295
DSP
0.882 0.080 6 7562999 intron variant T/G snv 0.46 3