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-04 107
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
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 29
rs113993959 0.677 0.280 7 117587778 stop gained G/A;T snv 8.0E-06; 3.4E-04 25
rs74597325 0.708 0.320 7 117587811 stop gained C/G;T snv 6.8E-05 18
rs2227956 0.752 0.400 6 31810495 missense variant G/A;C;T snv 0.87 12
rs1043618 0.752 0.280 6 31815730 5 prime UTR variant G/A;C;T snv 0.39; 2.0E-05; 4.0E-06 10
rs1061581 0.827 0.200 6 31816809 synonymous variant G/A snv 6
rs2076295
DSP
0.882 0.080 6 7562999 intron variant T/G snv 0.46 5