Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800206 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1803274 0.763 0.360 3 165773492 missense variant C/T snv 0.18 0.18 13
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs28936379 0.807 0.120 1 226888977 missense variant A/C;G;T snv 4.0E-06 10
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4151667 0.790 0.320 6 31946247 missense variant T/A snv 3.9E-02 3.4E-02 9
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs4746 0.708 0.400 6 38682852 missense variant T/A;G snv 0.36 21
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs746682028 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs7493 0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 24
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237