Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1047840 0.708 0.280 1 241878999 missense variant G/A snv 0.36 0.40 19
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs10889677 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs1200055659 0.851 0.080 1 153614902 missense variant G/A snv 7.0E-06 4
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs145204276 0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1884444 0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 34
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs5744174 0.742 0.360 1 223111186 missense variant A/G snv 0.39 0.34 13
rs621559 0.827 0.080 1 43179740 intron variant G/A snv 0.18 5
rs6682925 0.776 0.160 1 67165579 intron variant C/T snv 0.47 11
rs689466 0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 33
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs1143633 0.752 0.280 2 112832890 intron variant C/G;T snv 11
rs2241880 0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 37
rs2292832 0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs2303428 0.776 0.240 2 47476361 splice region variant T/A;C;G snv 4.0E-06; 0.12 9
rs3783553 0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins 26
rs3834129 0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 38