Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2023239 0.724 0.160 6 88150763 intron variant T/C snv 0.21 20
rs2197089 0.925 0.080 8 19968862 downstream gene variant G/A snv 0.61 5
rs2206277 0.925 0.080 6 50830813 intron variant C/T snv 0.19 4
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs2236242 0.776 0.280 14 94493715 intron variant T/A snv 0.31 9
rs2237895 0.790 0.240 11 2835964 intron variant A/C;T snv 10
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs2293855 0.851 0.120 8 11319901 non coding transcript exon variant G/A snv 0.35 5
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs2695121 0.716 0.280 19 50377484 5 prime UTR variant T/C snv 0.70 16
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18
rs3737787 0.763 0.280 1 161039733 3 prime UTR variant G/A snv 0.21 11
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs3782889 0.851 0.160 12 110912851 intron variant A/G snv 7.1E-02 5
rs3819024 0.701 0.560 6 52185988 upstream gene variant A/G snv 0.34 17
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4148325 0.851 0.080 2 233764663 intron variant C/T snv 0.36 11
rs4402960 0.724 0.400 3 185793899 intron variant G/T snv 0.38 21
rs45487298 0.882 0.120 1 209706871 intron variant -/A delins 3
rs4864548 0.827 0.160 4 55547636 non coding transcript exon variant G/A snv 0.33 8
rs5068 0.776 0.160 1 11845917 3 prime UTR variant A/G;T snv 13
rs512535 0.925 0.080 2 21044910 upstream gene variant T/C snv 0.45 3
rs518147 0.807 0.200 X 114584109 5 prime UTR variant C/A;G snv 7
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs670 0.763 0.360 11 116837697 5 prime UTR variant C/T snv 0.17 13