Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4073 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs735482 0.742 0.160 19 45408744 missense variant A/C snv 0.21 0.20 16
rs843720 0.752 0.280 2 54283523 intron variant T/G snv 0.52 10
rs937283 0.716 0.200 12 68808384 5 prime UTR variant A/G snv 0.37 19
rs145204276 0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480