Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs10865710 0.763 0.360 3 12311699 intron variant C/G snv 0.25 13
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26 27
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1232898090 0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 13
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
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
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1800730 0.649 0.480 6 26090957 missense variant A/T snv 1.0E-02 1.0E-02 32
rs1800777 0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02 17
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
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
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs243865 0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14