Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1567558 3 141289281 intron variant A/G snv 0.50 2
rs28721484 3 141334437 intron variant C/T snv 0.22 2
rs111906841 3 141242812 intron variant A/G snv 1.5E-02 1
rs55768579 3 141340945 intron variant GA/- delins 1.3E-03 1
rs34655123 3 141348246 intron variant A/G snv 4.7E-02 1
rs1346408 3 141353447 intron variant C/T snv 0.55 1
rs9866391 1.000 0.040 3 141357242 intron variant T/C snv 0.41 1