Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10036748 0.752 0.360 5 151078585 intron variant C/A;T snv 11
rs11221332 0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs11465804 0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 10
rs17293632 0.763 0.240 15 67150258 intron variant C/T snv 0.17 12
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1847472 0.807 0.200 6 90263440 intron variant C/A snv 0.25 7
rs2301436 0.752 0.320 6 167024500 intron variant C/T snv 0.42 11
rs3134792 0.851 0.280 6 31344549 intron variant T/G snv 8.8E-02 4
rs4129267 0.807 0.200 1 154453788 intron variant C/G;T snv 13
rs4696480 0.716 0.400 4 153685974 intron variant T/A snv 0.45 19
rs4845604 0.776 0.200 1 151829204 intron variant G/A;C;T snv 10
rs61839660 0.776 0.280 10 6052734 intron variant C/T snv 5.7E-02 9
rs628977 0.851 0.160 20 3669074 intron variant T/C snv 0.65 4
rs6908425 0.752 0.320 6 20728500 intron variant T/C snv 0.78 11
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 12
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 18
rs61816761 0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 43
rs11209026 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs11465553 0.925 0.120 6 52236960 missense variant C/T snv 3.0E-02 3.0E-02 2
rs11584340 0.827 0.200 1 152313454 missense variant G/A snv 0.27 0.19 5
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83