Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11580078 0.724 0.240 1 67203951 intron variant C/A;G snv 14
rs10889676 0.827 0.120 1 67256884 intron variant C/A;T snv 5
rs11209026 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs183686347 0.827 0.120 1 67237759 intron variant G/A snv 4.8E-03 5
rs80174646 0.827 0.120 1 67242472 intron variant G/T snv 5.8E-02 5
rs7517847 0.689 0.600 1 67215986 intron variant T/G snv 0.37 5
rs11581607 0.925 0.040 1 67242007 intron variant G/A snv 4.6E-02 4
rs2201841 0.716 0.440 1 67228519 intron variant A/G;T snv 3
rs10889677 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 2
rs76418789 0.882 0.080 1 67182913 missense variant G/A snv 7.3E-03 4.5E-03 2
rs1004819 0.776 0.360 1 67204530 intron variant G/A snv 0.30 1
rs11805303 0.827 0.240 1 67209833 intron variant C/T snv 0.30 1
rs11465804 0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 1
rs1343151 0.752 0.400 1 67253446 intron variant G/A snv 0.41 1