Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs132630304 0.882 0.080 X 150598660 missense variant C/G;T snv 1
rs132630305 1.000 0.080 X 150645725 missense variant C/T snv 1
rs132630307 1.000 0.080 X 150638967 missense variant G/A snv 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
rs587783759 1.000 0.080 X 150657927 missense variant C/A snv 1
rs587783762 1.000 0.080 X 150657972 missense variant G/C snv 1
rs587783764 1.000 0.080 X 150658000 missense variant G/T snv 1
rs587783772 0.776 0.200 X 150659665 missense variant G/A;T snv 1
rs587783796 1.000 0.080 X 150598600 missense variant G/A;T snv 1
rs587783801 1.000 0.080 X 150663460 missense variant T/C snv 1
rs587783809 1.000 0.080 X 150598663 missense variant C/T snv 1
rs587783816 1.000 0.080 X 150614617 missense variant T/C snv 1
rs587783832 1.000 0.080 X 150641275 missense variant C/T snv 1
rs587783835 1.000 0.080 X 150641290 missense variant A/G snv 1
rs587783836 1.000 0.080 X 150641297 missense variant C/T snv 1
rs587783841 1.000 0.080 X 150641354 missense variant C/T snv 1
rs587783848 1.000 0.080 X 150641416 missense variant C/A snv 1
rs587783850 1.000 0.080 X 150645683 missense variant G/A snv 1
rs587783851 1.000 0.080 X 150645687 missense variant T/C snv 1
rs587783856 1.000 0.080 X 150645795 missense variant T/G snv 1
rs781933660 1.000 0.080 X 150657977 missense variant G/A snv 1
rs886044782 1.000 0.080 X 150659694 missense variant G/A snv 1