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
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 21
rs1182188 0.827 0.120 7 2830351 intron variant T/C snv 0.26 7
rs34517439 0.882 0.120 1 77984833 intron variant C/A snv 7.3E-02 7
rs35874463 0.827 0.120 15 67165360 missense variant A/G snv 4.0E-02 3.4E-02 7
rs2066807 0.925 0.080 12 56346898 missense variant C/G snv 4.9E-02 4.6E-02 2
rs2066808 0.807 0.280 12 56344189 intron variant A/G snv 0.21 2
rs2778031 1.000 0.040 9 88220811 intergenic variant T/A;C snv 2