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 25
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 7
rs2650000 0.851 0.200 12 120951159 intron variant A/C snv 0.70 7