Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs111033313 0.925 0.160 7 107683453 splice acceptor variant A/G snv 3.6E-04 1.7E-04 4
rs121908363 0.925 0.160 7 107710126 missense variant C/T snv 5.2E-05 2.8E-05 4
rs192366176 0.925 0.160 7 107700180 splice region variant G/A snv 8.0E-06 1.4E-05 4
rs200455203 0.925 0.160 7 107701998 missense variant G/C snv 8.0E-06 1.4E-05 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
rs111033256 0.882 0.160 7 107675060 missense variant T/A snv 2.0E-04 3.5E-05 3
rs111033318 0.925 0.160 7 107702050 missense variant T/A snv 3
rs111033348 0.925 0.160 7 107674326 missense variant C/T snv 2.0E-05 7.0E-06 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
rs1241745103 0.925 0.160 7 107701139 frameshift variant G/- del 7.0E-06 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
rs747076316 0.925 0.160 7 107694622 stop gained C/A;G;T snv 2.0E-05 2.1E-05 3
rs752807925 0.925 0.160 7 107704382 stop gained C/T snv 1.3E-05 3