Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs6700896 0.827 0.160 1 65624099 intron variant C/T snv 0.44 9
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
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
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs3772622 0.851 0.080 3 148717966 intron variant T/A;C snv 4
rs3856806 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 41
rs5182 0.742 0.160 3 148741608 synonymous variant C/T snv 0.49 0.41 16
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs8192678 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
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
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs328
LPL
0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02 19
rs4149313 0.763 0.240 9 104824472 missense variant T/C snv 9
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182