Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4823006 22 29055683 3 prime UTR variant A/G snv 0.41 1
rs4055 22 28956507 intron variant A/C snv 0.13 1
rs13056243 22 28953318 intron variant C/T snv 0.13 1
rs16986864 22 28954923 intron variant G/T snv 0.13 1
rs5762862 22 28856744 intergenic variant G/A;T snv 1
rs16986861 22 28947200 intron variant G/A;C snv 0.13 1