Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs601338 0.742 0.280 19 48703417 stop gained G/A snv 0.38 0.45 19
rs7528684 0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 13
rs2281808 0.925 0.160 20 1629905 intron variant T/A;C snv 4