Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs9349379 0.732 0.200 6 12903725 intron variant A/G snv 0.32 19
rs2383206 0.742 0.320 9 22115027 intron variant A/G snv 0.49 17
rs2026458 0.882 0.080 6 12825642 intron variant C/T snv 0.34 6
rs9632884 0.851 0.160 9 22072302 intron variant G/A;C snv 6