Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1045933779 1.000 0.160 7 107710150 missense variant T/C snv 7.0E-06 1
rs1057516243 1.000 0.160 7 107698092 missense variant G/T snv 1
rs1057516354 1.000 0.160 7 107690212 frameshift variant A/- del 1
rs1057516535 1.000 0.160 7 107696030 splice donor variant TCAGTTGTGAGT/- delins 1
rs1057516634 1.000 0.160 7 107661696 frameshift variant A/- del 2.1E-05 1
rs1057516636 1.000 0.160 7 107701988 frameshift variant C/- delins 1
rs1057516658 1.000 0.160 7 107663380 stop gained G/A snv 1
rs1057516678 1.000 0.160 7 107674963 stop gained C/T snv 4.0E-06 1
rs1057516717 1.000 0.160 7 107695931 splice acceptor variant A/G snv 1
rs1057516796 1.000 0.160 7 107704363 frameshift variant T/- del 1
rs1057516881 1.000 0.160 7 107674350 splice donor variant T/A snv 1
rs1057516953 0.925 0.160 7 107663412 missense variant C/T snv 4.0E-06 3
rs1057516988 1.000 0.160 7 107674163 splice acceptor variant G/A snv 4.0E-06 1
rs1057517000 1.000 0.160 7 107690238 splice donor variant G/A;T snv 1
rs1057517042 1.000 0.160 7 107690147 missense variant C/A snv 1
rs1057517161 1.000 0.160 7 107701972 missense variant T/A snv 1
rs1057517246 1.000 0.160 7 107683290 frameshift variant GGAATTAA/- delins 1
rs1057517298 1.000 0.160 7 107694620 splice acceptor variant G/T snv 1
rs1057517303 0.925 0.160 7 107710192 stop gained T/A;C snv 3
rs1060499807 1.000 0.160 7 107689200 splice donor variant G/- delins 1
rs1060499808 0.925 0.160 7 107704344 missense variant T/C snv 8.9E-06 2
rs111033199 0.882 0.160 7 107672245 missense variant G/A;C;T snv 1.8E-04; 4.0E-06 3
rs111033200 1.000 0.160 7 107663301 stop gained C/A;G snv 1.2E-05 1
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