Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2447867 0.925 0.080 5 52861540 missense variant T/C;G snv 0.79; 4.0E-06 2
rs3815254 0.925 0.080 7 19943391 non coding transcript exon variant T/C;G snv 2
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs758272654 0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs1799964 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs763059810 0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs3804100 0.633 0.720 4 153704257 synonymous variant T/C snv 9.0E-02 6.7E-02 36
rs689466 0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 33
rs4833095 0.662 0.480 4 38798089 missense variant T/C snv 0.38 0.44 28
rs4778889 0.683 0.480 15 81296654 intron variant T/C snv 0.24 24
rs2296147 0.695 0.280 13 102846025 5 prime UTR variant T/C snv 0.38 21
rs1047768 0.695 0.320 13 102852167 synonymous variant T/C snv 0.52 0.59 20
rs1047972 0.716 0.240 20 56386407 missense variant T/C snv 0.85 0.84 19
rs16999593 0.742 0.240 19 10180505 missense variant T/C snv 2.4E-02 9.6E-03 14
rs13361189 0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21 13
rs667282 0.790 0.120 15 78571130 intron variant T/C snv 0.28 13
rs1342387 0.776 0.120 1 202945228 intron variant T/C snv 0.53 12
rs1665650 0.752 0.160 10 116727589 intron variant T/C snv 0.69 12
rs56250509 0.790 0.160 3 37014530 missense variant T/C snv 2.0E-05 10
rs1478604 0.807 0.240 15 39581120 5 prime UTR variant T/C snv 0.40 9