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
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
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
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs2234922 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 42
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
rs689466 0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 33
rs748500299 0.790 0.200 1 186675960 missense variant T/A;C snv 4.0E-06; 4.0E-06 8
rs9651118 0.683 0.480 1 11802157 intron variant T/C snv 0.18 20
rs10012 0.716 0.280 2 38075247 missense variant G/C snv 0.31 0.36 16
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs3783553 0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins 26
rs523349 0.689 0.440 2 31580636 missense variant G/A;C;T snv 0.66; 4.9E-06 21
rs6147150 0.827 0.160 2 211380365 3 prime UTR variant -/AAAATAGGATTG delins 5