Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3859192 0.925 0.080 17 39972395 intron variant C/T snv 0.42 3
rs3894194 0.882 0.120 17 39965740 missense variant G/A snv 0.46 0.41 2
rs3902025 0.925 0.080 17 39963001 intron variant G/T snv 0.56 2
rs6503526 0.925 0.080 17 39958345 intron variant C/T snv 0.41 2
rs1007654 1.000 0.080 17 39955101 intron variant A/G snv 0.69 1
rs7212938 0.925 0.120 17 39966427 missense variant G/A;C;T snv 4.1E-04; 4.2E-06; 0.52 1
rs7219080 1.000 0.080 17 39958263 intron variant A/C snv 0.65 1