Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs762846821 0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs2236225 0.614 0.640 14 64442127 missense variant G/A snv 0.44 0.38 52
rs397517132 0.623 0.280 7 55191846 missense variant A/T snv 48
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs1801157 0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16 46
rs12917 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45
rs1979277 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 45
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 44
rs11571833 0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 43
rs1800797 0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs1801155
APC
0.649 0.440 5 112839514 missense variant T/A snv 8.0E-06; 2.0E-03 1.2E-03 42