Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs768849283 0.882 0.040 10 70600517 missense variant C/G snv 6.8E-05 7
rs28933375 0.882 0.160 10 70598966 missense variant T/C snv 5.0E-03 7.5E-03 4
rs886042160 0.925 0.160 5 38511872 frameshift variant -/A delins 2
rs147462227 1.000 0.040 10 70600458 missense variant C/T snv 1.4E-04 7.0E-05 2
rs189650890 0.925 0.040 10 70598372 missense variant G/A snv 2.8E-05 2
rs28933973 1.000 0.040 10 70599048 missense variant G/A snv 1.2E-05 2
rs104894176 1.000 0.040 10 70598599 stop gained C/T snv 1.6E-05 2.8E-05 1
rs104894180 1.000 0.040 10 70600713 stop gained G/A;C snv 4.0E-06 1
rs104894181 1.000 0.040 10 70598435 missense variant C/T snv 4.0E-06 1
rs104894182 1.000 0.040 10 70598885 missense variant C/T snv 2.0E-05 1
rs104894183 1.000 0.040 10 70599173 missense variant A/C snv 1
rs1060499556 1.000 0.040 10 70598601 missense variant A/C;G snv 4.1E-06 1
rs138126912 1.000 0.040 10 70598411 missense variant G/A snv 7.3E-04 7.3E-04 1
rs147035858 1.000 0.040 10 70600853 frameshift variant A/- del 2.4E-04 9.8E-04 1
rs1554867753 1.000 0.040 10 70598546 frameshift variant G/- delins 1
rs1564723653 1.000 0.040 10 70598336 stop gained G/T snv 1
rs193302876 1.000 0.040 10 70598475 stop gained G/A snv 4.0E-06 1
rs28933374 1.000 0.040 10 70598687 missense variant G/A;T snv 4.0E-06 1
rs28933376 1.000 0.040 10 70598417 missense variant G/A snv 2.8E-05 1.4E-05 1
rs751161742 1.000 0.040 10 70598384 missense variant T/G snv 1.6E-05 1
rs751247865 1.000 0.040 10 70599055 missense variant G/T snv 3.6E-05 5.6E-05 1
rs752858869 1.000 0.040 10 70598640 missense variant T/A snv 8.1E-06 7.0E-06 1
rs771552960 1.000 0.040 10 70598630 frameshift variant AG/- del 1.2E-05 1
rs776299562 1.000 0.040 10 70600755 missense variant C/G;T snv 4.8E-05 1
rs786205093 1.000 0.040 10 70600696 frameshift variant G/- delins 7.0E-06 1