Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs431905486 0.925 0.160 7 107683531 frameshift variant -/A delins 2
rs786204450 1.000 0.160 7 107698042 frameshift variant -/C delins 1
rs768245266 1.000 0.160 7 107683351 frameshift variant -/G delins 1.2E-05 1
rs786204730 1.000 0.160 7 107672192 frameshift variant -/T delins 1
rs1298217152 1.000 0.160 7 107710138 frameshift variant -/TA delins 4.0E-06 7.0E-06 1
rs1057516354 1.000 0.160 7 107690212 frameshift variant A/- del 1
rs1057516634 1.000 0.160 7 107661696 frameshift variant A/- del 2.1E-05 1
rs918684449 1.000 0.160 7 107675077 frameshift variant A/- delins 1.2E-05 1.4E-05 1
rs1554360358 0.925 0.160 7 107698076 missense variant A/C snv 3
rs1413121429 1.000 0.160 7 107694619 splice acceptor variant A/C snv 7.0E-06 1
rs28939086 0.925 0.160 7 107690220 missense variant A/C;G snv 2.0E-04; 4.0E-06 4
rs201660407 0.925 0.160 7 107690236 missense variant A/C;G snv 8.0E-06; 1.2E-05 3
rs121908362 0.882 0.280 7 107710132 missense variant A/G snv 1.2E-04 3.5E-05 5
rs111033313 0.925 0.160 7 107683453 splice acceptor variant A/G snv 3.6E-04 1.7E-04 4
rs763006761 0.925 0.160 7 107700135 missense variant A/G snv 1.6E-05 3
rs397516411 0.925 0.160 7 107661637 splice acceptor variant A/G snv 1.2E-04 2.7E-04 2
rs757820624 0.925 0.160 7 107710135 missense variant A/G snv 2.0E-05 2.8E-05 2
rs760413427 0.925 0.160 7 107674187 missense variant A/G snv 8.0E-06 2
rs768471577 0.925 0.160 7 107694476 missense variant A/G snv 7.6E-05 2.1E-05 2
rs1057516717 1.000 0.160 7 107695931 splice acceptor variant A/G snv 1
rs111033244 1.000 0.160 7 107690125 missense variant A/G snv 1.1E-04 1.5E-04 1
rs111033316 1.000 0.160 7 107696036 missense variant A/G snv 5.6E-05 6.3E-05 1
rs142498437 1.000 0.160 7 107690212 missense variant A/G snv 8.0E-06 7.0E-06 1
rs1442599990 1.000 0.160 7 107672147 missense variant A/G snv 7.0E-06 1
rs397516424 1.000 0.160 7 107701986 missense variant A/G snv 2.8E-05 1.4E-05 1