Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs1047891 0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs1801253 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 34
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs1264347 1.000 0.040 6 30830920 upstream gene variant C/T snv 7.9E-02 4