Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7982
CLU
1.000 0.040 8 27604964 missense variant A/C;G snv 0.64 0.60 1
rs237025 0.672 0.360 6 149400554 missense variant G/A snv 0.55 0.57 26
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs12218 0.763 0.280 11 18269774 synonymous variant T/C snv 0.42 0.36 11
rs9331888 0.827 0.200 8 27611345 5 prime UTR variant C/G snv 0.35 0.28 5
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs3743930 0.611 0.720 16 3254626 missense variant C/G;T snv 7.1E-02 43
rs1800973
LYZ
0.827 0.320 12 69350234 missense variant C/A snv 4.2E-02 4.3E-02 9
rs4149584 0.683 0.440 12 6333477 missense variant C/G;T snv 4.0E-06; 1.3E-02 24
rs200538373 0.925 0.120 19 1061893 splice region variant G/A;C snv 2.5E-03 2
rs28940579 0.732 0.440 16 3243310 missense variant A/G;T snv 2.2E-03; 4.0E-06 13
rs28933981
TTR
0.807 0.200 18 31598647 missense variant C/T snv 1.5E-03 1.7E-03 8
rs76992529
TTR
0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03 36
rs121918095
TTR
0.827 0.160 18 31598602 missense variant G/A snv 7.9E-04 2.2E-04 6
rs121918074
TTR
0.851 0.120 18 31595247 missense variant C/A snv 6.0E-04 3.9E-04 5
rs63750847
APP
0.790 0.120 21 25897620 missense variant C/T snv 4.5E-04 3.0E-04 8
rs61752717 0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 72
rs28940578 0.716 0.400 16 3243405 missense variant C/T snv 1.4E-04 6.3E-05 16
rs28933979
TTR
0.587 0.600 18 31592974 missense variant G/A;C snv 1.0E-04 70
rs28940580 0.742 0.560 16 3243447 missense variant C/A;G;T snv 1.0E-04; 8.0E-06 17
rs759304648
GSN
0.790 0.240 9 121312479 synonymous variant G/A snv 8.0E-05 3.5E-05 9
rs121909211 0.724 0.200 5 136046407 missense variant G/A;T snv 4.0E-05 15
rs371792178 0.925 0.040 1 97699507 missense variant G/A;C snv 3.6E-05; 1.2E-05 3
rs766474822 0.925 0.080 6 43770990 missense variant G/A snv 1.4E-05 2.1E-05 2
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237