Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1420472625 0.925 0.040 19 54178800 missense variant G/C snv 2
rs1800234 0.807 0.240 22 46219983 missense variant T/A;C snv 4.0E-06; 1.1E-02 6
rs2070666 0.882 0.120 11 116830958 intron variant T/A;C snv 4
rs2228603 0.790 0.360 19 19219115 missense variant C/A;T snv 2.8E-05; 5.9E-02 12
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs2290602 0.882 0.040 4 23824109 intron variant T/A;G snv 3
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs641738 0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs72613567 0.742 0.320 4 87310240 splice donor variant -/A delins 0.22 14
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs74315468 0.882 0.040 22 50626841 missense variant G/A snv 4.0E-06 2.8E-05 3
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs1800777 0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02 17
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1800206 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs58542926 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs56225452 0.851 0.080 19 58513279 upstream gene variant C/T snv 0.18 5
rs12137855 0.882 0.040 1 219275036 downstream gene variant C/T snv 0.19 3
rs2896019 0.790 0.160 22 43937814 intron variant T/G snv 0.20 10
rs13361189 0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21 13
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 10
rs2143571 0.827 0.080 22 43995806 intron variant G/A snv 0.25 5