Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16857609 0.925 0.080 2 217431785 intron variant C/T snv 0.28 1
rs1351164 2 217407175 intron variant T/C snv 0.24 1
rs6435999 2 217658439 intron variant A/G snv 0.12 1
rs966423 0.776 0.200 2 217445617 intron variant C/G;T snv 1
rs6759952 1.000 0.080 2 217406996 intron variant T/A;C snv 1