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
rs2383206 0.742 0.320 9 22115027 intron variant A/G snv 0.49 17
rs1537372 0.752 0.120 9 22103184 intron variant G/A;T snv 14
rs10757269 1.000 0.040 9 22072265 intron variant A/C;G snv 4