Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72613567 0.742 0.320 4 87310240 splice donor variant -/A delins 0.22 14
rs2645424 0.827 0.120 8 11826954 intron variant A/C;G snv 0.56 5
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 10
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs58542926 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs641738 0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs2896019 0.790 0.160 22 43937814 intron variant T/G snv 0.20 10
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60