Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs646776 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 25
rs4803750 0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs1800775 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 18
rs6511720 0.790 0.120 19 11091630 intron variant G/T snv 0.12 15
rs1532085 0.882 0.080 15 58391167 intron variant A/G;T snv 13
rs1532624 0.851 0.160 16 56971567 intron variant C/A snv 0.34 12
rs1864163 0.882 0.120 16 56963321 intron variant G/A snv 0.26 10
rs7499892 16 56972678 intron variant C/G;T snv 7