Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs34637584 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs2075650 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs63750231 0.689 0.160 14 73198100 missense variant A/C;G snv 23
rs63750083 0.732 0.160 14 73219177 missense variant C/A;T snv 13