Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs80358284 0.790 0.240 11 86952443 missense variant T/A;C snv 4.0E-06; 2.4E-05 10
rs878853243 0.851 0.160 7 120806619 missense variant C/A snv 4
rs28933684 0.882 0.160 X 43949831 missense variant G/A;T snv 3
rs104894874 0.882 0.160 X 43958521 missense variant T/C snv 5.5E-06 3
rs727504031 0.925 0.200 X 43949981 missense variant G/A snv 3
rs104894876 0.925 0.160 X 43949873 missense variant A/C snv 2
rs758550101 0.925 0.160 X 43958534 missense variant G/A;T snv 5.5E-06; 5.5E-06 2
rs104894878 0.925 0.160 X 43949840 missense variant G/A snv 2
rs1460859456 0.925 0.160 X 43950001 missense variant C/A;T snv 2
rs774200714 1.000 0.160 11 86954909 missense variant G/T snv 3.6E-05 5.6E-05 1
rs104894870 1.000 0.160 X 43958515 missense variant T/C snv 1
rs104894872 1.000 0.160 X 43949995 missense variant C/G snv 1
rs104894873 1.000 0.160 X 43949817 stop gained G/A;T snv 3.1E-05 1
rs104894877 1.000 0.160 X 43949913 missense variant G/C snv 1
rs1057518793 1.000 0.160 X 43949933 missense variant G/A snv 1
rs137852221 1.000 0.160 X 43958512 missense variant A/T snv 1
rs104894867 1.000 0.160 X 43949932 missense variant C/A;G;T snv 1.2E-05; 2.4E-05 1
rs104894868 1.000 0.160 X 43949977 missense variant G/C snv 1
rs104894869 1.000 0.160 X 43950022 missense variant A/T snv 1
rs104894871 1.000 0.160 X 43949914 missense variant C/T snv 1
rs104894875 1.000 0.160 X 43949888 missense variant C/A;T snv 1
rs104894879 1.000 0.160 X 43958608 missense variant A/C snv 1
rs104894880 1.000 0.160 X 43950020 missense variant G/A snv 1
rs104894882 1.000 0.160 X 43949983 stop gained G/T snv 1
rs104894883 1.000 0.160 X 43949899 missense variant G/A snv 1