Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs11833579 0.827 0.200 12 666033 upstream gene variant G/A snv 0.25 6
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs746682028 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs4746 0.708 0.400 6 38682852 missense variant T/A;G snv 0.36 21
rs1138272 0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs9268877 0.827 0.200 6 32463370 intron variant A/G;T snv 5
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs4072111 0.716 0.400 15 81285798 missense variant C/T snv 0.17 0.11 16
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1800587 0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs8702 0.851 0.160 14 103686015 3 prime UTR variant C/G snv 0.61 5