Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs3828805 0.752 0.160 6 32668343 5 prime UTR variant T/A;C snv 12
rs1961637 0.827 0.160 2 223040390 regulatory region variant G/T snv 0.59 5
rs17358800 0.827 0.160 1 110235437 3 prime UTR variant A/G snv 0.21 5
rs6847067 0.827 0.160 4 84811016 intron variant C/A snv 0.39 5