Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3131296 0.807 0.320 6 32205216 intron variant C/T snv 0.11 6
rs7762279 0.807 0.360 6 32787513 intergenic variant T/C snv 8.4E-02 6
rs13211507 0.882 0.200 6 28289600 intron variant T/C snv 6.4E-02 4
rs10484399 0.851 0.240 6 27566749 intergenic variant A/G snv 5.4E-02 3