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
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 28
rs708272 0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 24
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs12149545 0.851 0.080 16 56959249 upstream gene variant G/A snv 0.23 7