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
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs3918242 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs1202989817 0.716 0.360 21 31659813 missense variant T/C;G snv 8.0E-06 7.0E-06 18