Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 39
rs3087243 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 12
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 11
rs1495741 0.827 0.240 8 18415371 regulatory region variant G/A snv 0.71 6
rs4148323 0.701 0.440 2 233760498 missense variant G/A snv 2.2E-02 9.2E-03 6
rs2741045 2 233671494 intron variant C/T snv 0.22 3
rs9274407 0.925 0.120 6 32665055 missense variant A/C;T snv 0.77 2
rs17036170 1.000 0.080 3 12288912 5 prime UTR variant G/A snv 1.1E-02 2
rs116561224 1.000 0.080 18 66962261 intergenic variant A/G snv 7.4E-02 1
rs72631567 1.000 0.080 2 5092045 intergenic variant A/G snv 4.5E-02 1
rs2287622 0.724 0.240 2 168973818 missense variant A/C;G;T snv 0.57 1
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 1
rs114577328 1.000 0.080 6 29959505 downstream gene variant G/C snv 1.3E-02 1
rs3135388 0.807 0.240 6 32445274 downstream gene variant A/G snv 0.90 1