Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs2071746 0.708 0.320 22 35380679 intron variant A/T snv 0.49 18
rs213045 0.851 0.120 1 21290752 intron variant G/T snv 0.44 5
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs11542041 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 23
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1314386070 0.827 0.240 8 90042766 missense variant T/C snv 1.4E-05 9
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800206 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs2043211 0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 29
rs2066714 0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25 13
rs2066715 0.807 0.160 9 104825752 missense variant C/T snv 8.2E-02 5.5E-02 7
rs2230806 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4149313 0.763 0.240 9 104824472 missense variant T/C snv 9