Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1210484348 0.925 0.080 9 130884973 missense variant C/T snv 7.0E-06 3
rs143683481 1.000 0.080 2 26278736 missense variant G/A snv 9.1E-05 3.1E-04 1
rs750956714 1.000 0.080 2 26277125 missense variant T/C snv 4.0E-06 1
rs1367079155 1.000 0.080 4 99594764 missense variant G/C snv 4.0E-06 1
rs146064714 1.000 0.080 4 99622756 stop gained G/T snv 1.2E-04 3.5E-05 1
rs1485375137 1.000 0.080 4 99608790 missense variant T/C snv 7.0E-06 1
rs1553926818 1.000 0.080 4 99591735 frameshift variant CA/- delins 1
rs1553927840 1.000 0.080 4 99608764 splice acceptor variant A/G snv 1
rs1560614154 1.000 0.080 4 99582057 frameshift variant C/- delins 1
rs1560614646 1.000 0.080 4 99583431 stop gained A/T snv 1
rs1560621444 1.000 0.080 4 99601606 splice acceptor variant G/A snv 1
rs1560621495 1.000 0.080 4 99601674 missense variant T/A snv 1
rs199422219 1.000 0.080 4 99611156 stop gained C/T snv 7.0E-06 1
rs199422220 1.000 0.080 4 99608827 missense variant G/A snv 1.6E-05 3.5E-05 1
rs199422221 1.000 0.080 4 99619094 missense variant A/T snv 1
rs199422222 1.000 0.080 4 99608977 missense variant G/T snv 1
rs372321643 1.000 0.080 4 99608826 missense variant C/T snv 2.8E-05 4.2E-05 1
rs755681036 1.000 0.080 4 99613134 frameshift variant T/- delins 1
rs767833468 1.000 0.080 4 99618993 missense variant G/A snv 4.0E-06 1