Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801278 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 36
rs1801276 0.882 0.160 2 226797205 missense variant C/G snv 1.4E-02 1.3E-02 3
rs13431554 0.925 0.120 2 226732872 3 prime UTR variant A/G snv 0.10 2
rs104893642 1.000 0.080 2 226796916 missense variant G/A;C snv 1.5E-05; 5.0E-06 1
rs10498210 1.000 0.080 2 226755230 intron variant G/A snv 9.0E-02 1
rs1801118 1.000 0.080 2 226798113 missense variant A/G snv 5.6E-05 2.1E-05 1
rs1801120 1.000 0.080 2 226796313 missense variant G/A snv 4.0E-06 1