Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 131
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 127
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 118
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 117
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 114
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 110
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 110
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 107
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 103
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 98
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 97
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 97
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 93
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 92
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 91
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 86