Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7137828 0.763 0.200 12 111494996 intron variant C/A;T snv 14
rs604723 1.000 0.040 11 100739815 intron variant T/C snv 0.78 8
rs13139571 1.000 0.040 4 155724361 intron variant C/A snv 0.22 7
rs7209400 1.000 0.040 17 49372695 intron variant C/T snv 0.47 6