Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs2231142 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56