Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17154929 1.000 0.160 10 44029227 intergenic variant C/T snv 2.3E-02 1
rs12742923 1.000 0.160 1 83024161 intron variant C/T snv 0.13 1
rs7996217 1.000 0.160 13 101348594 intron variant T/G snv 1.6E-02 1
rs404005 1.000 0.160 2 40168938 intron variant C/T snv 0.59 1