Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11045879 1.000 0.120 12 21229685 intron variant T/C snv 0.18 4
rs751837 0.882 0.120 14 103018488 intron variant T/C snv 0.23 4
rs143002189 1.000 0.120 6 137881310 missense variant G/A snv 4.3E-04 4.4E-04 3
rs587781386 0.882 0.120 17 7674889 missense variant A/C;G snv 3.2E-05; 4.0E-06 3
rs764562217 0.882 0.120 17 7673308 stop lost T/G snv 2.3E-05 3.5E-05 3
rs8094402
MBP
0.882 0.120 18 76995493 intron variant A/G snv 0.25 3
rs9831894 0.882 0.120 3 122081640 intron variant A/C snv 0.31 3
rs111724149 0.925 0.120 11 45204720 missense variant A/G snv 1.8E-03 1.8E-03 2
rs1227230819 0.925 0.120 5 37815877 missense variant T/C snv 4.0E-06 2
rs1239470707 0.925 0.120 3 12416785 missense variant C/A snv 2
rs1312391542 0.925 0.120 6 106104897 missense variant G/A;T snv 2
rs13255292 0.925 0.120 8 128064327 intron variant C/T snv 0.24 2
rs1390458638 0.925 0.120 2 219216441 missense variant G/A snv 4.0E-06 2
rs1443292790 1.000 0.120 17 63929438 missense variant T/C snv 2
rs1880030 0.925 0.120 12 122046634 intron variant G/A snv 0.39 2
rs2070770 0.925 0.120 11 60463058 synonymous variant C/T snv 7.1E-02 5.4E-02 2
rs2681416 0.925 0.120 3 122098766 intron variant G/A snv 0.26 2
rs3025684 1.000 0.120 16 3745362 splice region variant G/A snv 7.7E-02 0.15 2
rs3218674
ATM
1.000 0.120 11 108244860 synonymous variant C/G;T snv 1.1E-02 1.1E-02 2
rs35090414 0.925 0.120 11 45224227 missense variant G/A;T snv 1.5E-04; 8.2E-02 2
rs3813729
C1RL ; C1R
0.925 0.120 12 7089608 missense variant C/G;T snv 2
rs6773854 1.000 0.120 3 187931631 downstream gene variant T/C snv 0.23 2
rs758653954
EFS
0.925 0.120 14 23357350 frameshift variant -/C delins 4.0E-06; 8.0E-06 2
rs770027749 0.925 0.120 22 28795623 missense variant C/A;G snv 8.0E-06 2
rs7712513 0.925 0.120 5 122582513 intergenic variant G/T snv 0.71 2