Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs200034765 10 69247416 missense variant C/T snv 1.2E-05 2.1E-05 1
rs1564726619 10 69232838 missense variant G/T snv 1
rs1563293555 8 42930130 missense variant T/G snv 1
rs747141054 8 42973316 missense variant G/A snv 2.4E-05 4.9E-05 1
rs143130309 12 110163027 missense variant C/A;T snv 2.0E-05 1
rs761469100 12 110128960 missense variant C/T snv 1.2E-05 1
rs761191483 X 54757697 stop gained G/A;C snv 5.4E-06 1
rs376253982 X 48966313 splice region variant C/A snv 2.0E-04 2.1E-04 1
rs370433088 20 62322314 missense variant C/T snv 1.0E-04 1.0E-04 1
rs773956500 20 62322722 missense variant T/C snv 4.3E-05 2.9E-05 1
rs782144677 1 147285398 frameshift variant A/- del 2.8E-05 2.1E-05 1
rs1567966432 18 21383629 missense variant T/G snv 1
rs377314861 18 21440307 missense variant C/T snv 6.3E-06 1
rs1569197778 X 55488927 stop gained G/A snv 1
rs1569405174 X 110317618 frameshift variant G/- delins 1
rs1469540056 22 20982433 missense variant G/C;T snv 5.1E-06 1
rs559634261 1 39318497 missense variant G/A snv 2.0E-05 1
rs755081350 1 39485559 missense variant G/A snv 1.6E-05 1
rs1568162263 17 40029767 missense variant G/C snv 1
rs760297650 17 40022789 missense variant C/T snv 2.0E-05 2.1E-05 1
rs766464011 20 62333128 missense variant G/T snv 1.1E-04 5.6E-05 1
rs1558553140 2 42659795 missense variant G/A snv 1
rs1430282035 20 34996388 missense variant G/A snv 8.3E-06 1
rs771172991 20 34987284 splice donor variant AG/- delins 5.6E-05 1
rs1158061584 13 32443086 frameshift variant T/-;TT delins 1