Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17038466 1.000 0.040 3 39101997 intron variant A/G snv 3.4E-02 1
rs3732377 1.000 0.040 3 39097349 3 prime UTR variant A/G snv 0.10 1
rs4676631 1.000 0.040 3 39101632 intron variant T/C snv 3.4E-02 1