Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2505083 0.882 0.080 10 30046193 intron variant T/C snv 0.33 2
rs1887318 1.000 0.040 10 30032669 intron variant C/T snv 0.34 1
rs2487928 1.000 0.040 10 30034963 intron variant G/A snv 0.34 1
rs9337951 1.000 0.040 10 30028144 synonymous variant G/A snv 0.27 0.25 1