Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs763006761 0.925 0.160 7 107700135 missense variant A/G snv 1.6E-05 3
rs786204474 0.925 0.160 7 107689130 missense variant C/T snv 7.0E-06 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
rs912147281 0.925 0.160 7 107683356 splice donor variant T/C snv 8.0E-06 1.4E-05 3
rs1057516953 0.925 0.160 7 107663412 missense variant C/T snv 4.0E-06 3
rs786204581 0.925 0.160 7 107663366 stop gained C/T snv 3
rs1060499808 0.925 0.160 7 107704344 missense variant T/C snv 8.9E-06 2
rs111033257 0.925 0.160 7 107700162 missense variant G/A snv 1.4E-05 2
rs111033303 0.925 0.160 7 107674970 missense variant G/T snv 3.0E-04 3.8E-04 2
rs111033308 0.925 0.160 7 107695984 missense variant G/A;C snv 2.0E-05 6.3E-05 2
rs121908365 0.925 0.160 7 107672230 missense variant T/A;C snv 2
rs145254330 0.925 0.160 7 107672182 missense variant C/T snv 3.3E-04 1.7E-04 2
rs146281367 0.925 0.160 7 107683537 missense variant G/A;C;T snv 4.0E-06; 8.0E-06 2
rs1554354787 0.925 0.160 7 107674188 missense variant T/C snv 2
rs1554359670 0.925 0.160 7 107694650 missense variant C/A snv 2
rs397516413 0.925 0.160 7 107690171 frameshift variant T/- delins 7.0E-06 2
rs397516414 0.925 0.160 7 107690178 missense variant G/A snv 2
rs431905486 0.925 0.160 7 107683531 frameshift variant -/A delins 2
rs542620119 0.925 0.160 7 107674302 missense variant G/C snv 9.1E-05 3.5E-05 2