Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs111033205 0.882 0.240 7 107661726 stop gained G/C;T snv 9.3E-05; 6.2E-06 4
rs111033212 0.851 0.240 7 107689054 missense variant T/A;C snv 4.0E-06; 8.6E-04 4
rs111033220 0.925 0.160 7 107690203 missense variant C/G;T snv 4.0E-06; 1.8E-04 4
rs111033305 0.925 0.160 7 107690200 missense variant G/A;C snv 1.0E-04; 8.0E-06 4
rs111033312 0.925 0.160 7 107698112 splice donor variant G/A;C;T snv 1.6E-05; 4.0E-06 4
rs201562855 0.925 0.160 7 107690148 missense variant A/T snv 4.0E-06 4
rs28939086 0.925 0.160 7 107690220 missense variant A/C;G snv 2.0E-04; 4.0E-06 4
rs539699299 0.851 0.160 7 107661725 missense variant C/A;G snv 4
rs1057516953 0.925 0.160 7 107663412 missense variant C/T snv 4.0E-06 3
rs1057517303 0.925 0.160 7 107710192 stop gained T/A;C snv 3
rs111033199 0.882 0.160 7 107672245 missense variant G/A;C;T snv 1.8E-04; 4.0E-06 3
rs111033242 0.925 0.160 7 107675050 missense variant C/G snv 4.8E-05 3
rs111033318 0.925 0.160 7 107702050 missense variant T/A snv 3
rs121908361 0.882 0.160 7 107689156 stop gained A/G;T snv 3
rs121908364 0.925 0.160 7 107689166 missense variant C/T snv 3
rs147952620 0.925 0.160 7 107690199 missense variant C/T snv 1.6E-05 3
rs1554360358 0.925 0.160 7 107698076 missense variant A/C snv 3
rs201660407 0.925 0.160 7 107690236 missense variant A/C;G snv 8.0E-06; 1.2E-05 3
rs752807925 0.925 0.160 7 107704382 stop gained C/T snv 1.3E-05 3
rs763006761 0.925 0.160 7 107700135 missense variant A/G snv 1.6E-05 3
rs786204581 0.925 0.160 7 107663366 stop gained C/T snv 3
rs786204601 0.925 0.160 7 107696014 frameshift variant T/- delins 3
rs786204739 0.925 0.160 7 107698083 missense variant T/G snv 3
rs1060499808 0.925 0.160 7 107704344 missense variant T/C snv 8.9E-06 2
rs121908365 0.925 0.160 7 107672230 missense variant T/A;C snv 2