Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs587783772 0.776 0.200 X 150659665 missense variant G/A;T snv 14
rs1057516031 1.000 0.080 X 150598681 stop gained G/T snv 3
rs132630304 0.882 0.080 X 150598660 missense variant C/G;T snv 3
rs587783752 0.925 0.080 X 150657854 frameshift variant AA/-;AAA delins 2
rs132630302 1.000 0.080 X 150641306 missense variant A/G snv 1
rs132630303 1.000 0.080 X 150657957 missense variant A/G snv 1
rs132630305 1.000 0.080 X 150645725 missense variant C/T snv 1
rs132630306 1.000 0.080 X 150641410 stop gained C/T snv 1
rs132630307 1.000 0.080 X 150638967 missense variant G/A snv 1
rs1557413092 1.000 0.080 X 150614700 splice donor variant G/A snv 1
rs1557413783 1.000 0.080 X 150638963 frameshift variant T/- del 1
rs1557414513 1.000 0.080 X 150657943 frameshift variant -/T delins 1
rs1569565497 1.000 0.080 X 150641333 missense variant A/C snv 1
rs1569565525 1.000 0.080 X 150657971 missense variant G/A snv 1
rs34119065 1.000 0.080 X 150671572 frameshift variant C/-;CC delins 1
rs397518445 1.000 0.080 X 150659654 intron variant A/G snv 1
rs398123274 1.000 0.080 X 150645692 missense variant T/C snv 1
rs398123275 1.000 0.080 X 150596504 stop gained C/T snv 1
rs587783750 1.000 0.080 X 150649884 missense variant T/C snv 1
rs587783751 1.000 0.080 X 150649902 splice donor variant G/A;C snv 1
rs587783753 1.000 0.080 X 150596543 stop gained C/T snv 9.5E-06 1
rs587783754 1.000 0.080 X 150657887 missense variant C/G snv 1
rs587783755 1.000 0.080 X 150657899 missense variant G/A snv 1
rs587783756 1.000 0.080 X 150657903 stop gained G/A snv 1
rs587783757 1.000 0.080 X 150657904 stop gained G/A snv 1