Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs559972 17 29487478 intron variant C/T snv 0.38 1
rs7213208 17 29405851 intron variant A/G;T snv 1
rs7208363 17 29406390 intron variant A/G;T snv 1
rs9900280 17 29442580 intron variant G/A snv 0.58 1