Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 26
rs6993770 0.925 0.080 8 105569300 intron variant A/T snv 0.31 7
rs11553699 12 121779004 3 prime UTR variant A/G snv 9.4E-02 6
rs1801689 17 66214462 missense variant A/C;G snv 4.0E-06; 2.4E-02; 4.8E-05 5
rs17580 0.776 0.160 14 94380925 missense variant T/A snv 2.3E-02 2.9E-02 4
rs8176747
ABO
9 133255928 missense variant C/A;G snv 4.1E-06; 0.12 4
rs72835078 17 4923297 intron variant G/T snv 0.14 2