Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs1800925 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs324011 0.742 0.360 12 57108399 intron variant C/T snv 0.32 12
rs8113232 0.925 0.160 19 3586545 synonymous variant G/A snv 4.0E-06; 0.14 0.24 3