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 0.93 121
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs3087243 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 44
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs6679677 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 26
rs34536443 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 25
rs17696736 0.827 0.240 12 112049014 intron variant A/G snv 0.30 18
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 17
rs2516049 0.742 0.400 6 32602623 intergenic variant T/C snv 0.27 12
rs477515 0.790 0.400 6 32601914 intergenic variant G/A snv 0.27 10
rs6910071 0.790 0.320 6 32315077 intron variant A/G snv 0.14 7
rs7090530 0.851 0.160 10 6068912 downstream gene variant C/A snv 0.59 4
rs2517532 0.925 0.120 6 31050630 upstream gene variant A/G snv 0.60 2