Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2477686 0.807 0.040 1 2461209 intron variant G/C snv 0.64 7
rs10842262 0.851 0.040 12 24031610 intron variant G/C snv 0.43 5
rs6080550 0.851 0.040 20 1778944 intron variant C/G;T snv 9.6E-02 5
rs12097821 0.882 0.040 1 106793679 regulatory region variant G/A;T snv 4
rs140506267 0.925 0.040 9 894044 missense variant A/G snv 2.7E-03 1.3E-03 2