Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1887922
IDE
0.851 0.240 10 92464408 intron variant C/T snv 0.85 6
rs2227564 0.763 0.320 10 73913343 missense variant T/C snv 0.75 0.81 12
rs1570360 0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 107
rs3734254 0.752 0.240 6 35427233 3 prime UTR variant C/T snv 0.69 13
rs2233679 0.763 0.360 19 9834678 splice region variant C/T snv 0.59 11
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 153
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 80
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs2230806 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs11568820
VDR
0.672 0.480 12 47908762 intron variant C/T snv 0.38 27
rs2236225 0.614 0.640 14 64442127 missense variant G/A snv 0.44 0.38 51
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 187
rs4986938 0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33 35
rs1800587 0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 59
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 169
rs2333227
MPO
0.752 0.320 17 58281401 upstream gene variant C/T snv 0.24 15