Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9383938 0.827 0.160 6 151666222 intron variant G/T snv 0.11 2
rs139960913 1.000 0.080 6 151807928 missense variant C/T snv 3.3E-03 3.1E-03 1
rs3798758 0.925 0.080 6 152100719 3 prime UTR variant C/A snv 7.4E-02 1
rs796065354 0.882 0.080 6 151944320 missense variant A/G snv 1