Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs6548238 0.882 0.200 2 634905 TF binding site variant T/C snv 0.85 10
rs822396 0.732 0.400 3 186849088 intron variant G/A snv 0.81 16
rs2016520 0.752 0.320 6 35411001 5 prime UTR variant C/T snv 0.78 16
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
rs3736544 0.882 0.160 4 55443825 synonymous variant A/G snv 0.70 0.69 4
rs5082 0.807 0.160 1 161223893 upstream gene variant G/A snv 0.68 8
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs10010131 0.827 0.120 4 6291188 intron variant A/G snv 0.66 0.63 7
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs20455 0.763 0.160 6 39357302 missense variant A/G snv 0.41 0.49 12
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1333048 0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs660339 0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43 24
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs659366 0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40 17
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32