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
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs4803750 0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs2650000 0.851 0.200 12 120951159 intron variant A/C snv 0.70 10
rs612169
ABO
9 133268030 intron variant G/A snv 10
rs10096633 1.000 0.040 8 19973410 regulatory region variant C/T snv 0.22 8