Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2292832 0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs2043211 0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 29
rs10754558 0.695 0.480 1 247448734 3 prime UTR variant G/C;T snv 20
rs1239681664 0.716 0.320 9 104818690 synonymous variant A/G snv 7.0E-06 15
rs2227564 0.763 0.320 10 73913343 missense variant T/C snv 0.75 0.81 15
rs17293632 0.763 0.240 15 67150258 intron variant C/T snv 0.17 12
rs2277680 0.776 0.160 17 4735268 missense variant G/A snv 0.47 0.41 10