Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1709183 0.882 0.160 6 151872861 intron variant C/T snv 0.67 3
rs1749824 0.925 0.080 10 79164105 intron variant C/A snv 0.39 3
rs1952034 0.882 0.160 14 59691018 intron variant C/T snv 0.35 3
rs2032487 0.882 0.080 22 36299382 intron variant C/T snv 0.78 3
rs2431260 0.882 0.160 6 151871196 intron variant G/C;T snv 3
rs2720709 0.882 0.160 8 128046110 intron variant G/A;C snv 3
rs41302867 0.925 0.080 6 7240643 intron variant G/A snv 8.5E-02 8.2E-02 3
rs4281481 0.882 0.080 11 22859013 intron variant C/G snv 0.36 3
rs926632 0.882 0.160 20 59309707 intron variant C/T snv 0.61 3
rs12431381 0.925 0.080 14 59643053 intron variant T/C snv 0.35 2
rs12437854 0.925 0.080 15 93598604 intron variant T/G snv 0.10 2
rs12917114 0.925 0.080 15 47852953 intron variant C/T snv 8.9E-02 2
rs1516792 0.925 0.080 2 112778356 intron variant G/A snv 2
rs17709344 0.925 0.080 15 93608310 intron variant G/A snv 4.0E-02 2
rs183962941 0.925 0.080 16 20343125 intron variant G/A snv 1.1E-02 2
rs2413396 0.925 0.080 22 36312039 intron variant C/G;T snv 0.88 2
rs2802723 0.925 0.080 1 243335010 intron variant T/C;G snv 2
rs2838302 0.925 0.080 21 43419273 intron variant A/G snv 1.0E-01 2
rs301640 0.925 0.080 13 60885853 intron variant C/G;T snv 2
rs373971520 0.925 0.080 19 2568808 intron variant CA/-;CACA delins 2
rs6936632 0.925 0.080 6 47588297 intron variant G/A snv 7.6E-02 2
rs702483 0.925 0.080 7 6387310 intron variant C/A;T snv 0.54 2
rs7583877 0.925 0.080 2 99844192 intron variant C/T snv 0.61 2
rs7918972 0.925 0.080 10 16828293 intron variant T/G snv 0.15 2
rs836488 0.925 0.080 7 6380162 intron variant C/T snv 0.13 2