Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35388001 17 49779962 intron variant C/T snv 0.20 2
rs79041579 17 49783553 intron variant G/A snv 0.15 2
rs1123339 17 49789170 non coding transcript exon variant G/A snv 6.6E-02 2
rs575705078 17 49779547 intron variant A/G snv 6.1E-04 1