Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs11575937 0.653 0.480 1 156136985 missense variant G/A;T snv 29
rs2004640 0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 26
rs1799895 0.683 0.360 4 24800212 missense variant C/G snv 2.3E-02 1.2E-02 26
rs35829419 0.689 0.560 1 247425556 missense variant C/A snv 3.9E-02 3.3E-02 23
rs2276109 0.701 0.440 11 102875061 upstream gene variant T/C snv 9.2E-02 18
rs1022113606 0.732 0.280 4 24800161 missense variant G/C snv 1.6E-04 2.1E-05 17
rs35705950 0.763 0.240 11 1219991 splice region variant G/A;T snv 14
rs652438 0.716 0.400 11 102865911 missense variant T/C;G snv 7.1E-02; 2.5E-04 14
rs727088 0.790 0.400 18 69863203 3 prime UTR variant G/A snv 0.47 8
rs10168266 0.776 0.400 2 191071078 intron variant C/T snv 0.19 8
rs1059702 0.807 0.280 X 154018741 missense variant A/G snv 0.72 7
rs121917737 0.827 0.080 10 79557264 missense variant C/A snv 5
rs121917738 0.827 0.080 10 79557363 missense variant A/G snv 5
rs2609255 0.882 0.080 4 88890044 intron variant G/T snv 0.73 4
rs6837671 0.925 0.040 4 88951941 intron variant A/G snv 0.47 4
rs587777609 0.851 0.040 5 139480849 missense variant T/C snv 4
rs2241718 0.882 0.040 19 41323701 3 prime UTR variant G/A snv 0.15 4
rs3917200 0.882 0.080 14 75963525 intron variant A/G snv 9.2E-02 0.14 3
rs34794968 0.925 0.200 18 69863790 3 prime UTR variant C/A snv 0.36 2
rs2034650
IVD
1.000 0.040 15 40425103 intron variant G/A snv 0.46 2
rs1433372015 0.925 0.040 5 139480855 missense variant T/C snv 7.0E-06 2
rs141425941 0.925 0.040 5 1272196 missense variant C/T snv 9.0E-05 1.5E-04 2