Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7034200 1.000 0.080 9 4289050 intron variant C/A;G snv 3
rs10814916 0.851 0.200 9 4293150 intron variant A/C snv 0.57 2
rs10758593 0.827 0.240 9 4292083 intron variant G/A snv 0.45 1
rs4237150 9 4290085 intron variant G/A;C;T snv 1