Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs2670660 0.708 0.400 17 5615686 intron variant A/G snv 0.41 15
rs3917887 0.776 0.240 17 34255979 non coding transcript exon variant AGCTCCTCCTTCTC/-;AGCTCCTCCTTCTCAGCTCCTCCTTCTC delins 0.33 8
rs12976445 0.689 0.600 19 51693200 non coding transcript exon variant T/C snv 0.45 20
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73