Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs148704956 0.716 0.360 6 52187772 missense variant A/G snv 8.0E-06 7.0E-06 19
rs4975616 0.763 0.320 5 1315545 downstream gene variant G/A snv 0.51 12
rs1864183 0.742 0.240 5 82253397 missense variant C/T snv 0.52 0.40 12
rs989902 0.742 0.240 4 86785353 missense variant T/G snv 0.42 0.53 12
rs28366003 0.763 0.240 16 56608579 upstream gene variant A/C;G snv 4.6E-02 10
rs115160714 0.807 0.200 3 133601021 3 prime UTR variant G/A snv 5.8E-03 9
rs6877842 0.807 0.320 5 31532531 intron variant G/C snv 0.16 7
rs820196 0.807 0.160 17 75631459 missense variant T/A;C snv 1.6E-05; 0.26 6
rs5744455 0.882 0.160 5 140633722 upstream gene variant G/A;T snv 5
rs13078 0.827 0.280 14 95090410 3 prime UTR variant A/T snv 0.85 5
rs2230600 0.827 0.160 4 86769845 missense variant A/G snv 0.18 0.14 5
rs4789223 0.851 0.120 17 75645819 intron variant G/A snv 0.46 4
rs4253211 0.882 0.240 10 49470271 missense variant C/G;T snv 7.1E-02; 2.0E-05 3
rs1816158 0.925 0.200 11 122155752 intron variant C/A;T snv 3
rs3213282 0.882 0.160 19 43568728 intron variant G/C snv 0.57 3
rs3810378 1.000 0.120 19 43577449 intron variant G/C snv 0.29 3
rs748148861 0.925 0.120 6 167136856 missense variant G/C snv 8.0E-06 2
rs50871 0.925 0.120 19 45359257 intron variant C/A snv 0.64 2
rs4725443 0.925 0.120 7 152170176 intron variant T/C snv 9.3E-02 2
rs6464211 0.925 0.160 7 152176768 synonymous variant C/T snv 0.24 0.34 2
rs6943984 0.925 0.120 7 152201919 intron variant G/A snv 0.11 2
rs28903090 0.925 0.120 5 132587981 missense variant G/T snv 1.2E-03 1.4E-03 2
rs56161233 0.925 0.120 2 235055489 3 prime UTR variant C/T snv 0.11 2
rs865789884 0.925 0.120 8 23145778 missense variant G/A;C snv 4.0E-06 2
rs1799778 1.000 0.120 19 43554989 intron variant G/T snv 0.31 1