Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2664581
PI3
0.882 0.120 20 45175881 missense variant A/C snv 0.16 0.16 3
rs3774934 0.851 0.080 4 102506319 intron variant A/C;G;T snv 4
rs12252 0.695 0.240 11 320772 splice region variant A/G snv 0.13 0.13 23
rs1051931 0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs1805018 0.827 0.200 6 46711566 missense variant A/G snv 6.8E-02 0.10 6
rs7744 0.827 0.160 3 38142530 3 prime UTR variant A/G snv 0.13 5
rs1042689672 0.925 0.080 10 79557504 missense variant A/G snv 7.0E-06 2
rs7692976
EGF
1.000 0.040 4 109990411 intron variant A/G;T snv 2
rs4698803
EGF
1.000 0.040 4 109993271 missense variant A/G;T snv 0.85 1
rs13402990 1.000 0.040 2 70231632 intron variant A/T snv 9.7E-03 1
rs2277212 1.000 0.040 10 11257772 synonymous variant A/T snv 0.75 0.74 1
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs2606345 0.732 0.360 15 74724835 intron variant C/A snv 0.46 16
rs10905928 1.000 0.040 10 11300924 intron variant C/A snv 0.21 1
rs672961 1.000 0.040 1 70101505 intron variant C/G snv 0.99 1
rs1800972 0.708 0.440 8 6877901 5 prime UTR variant C/G;T snv 0.79 16
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs1800450 0.662 0.640 10 52771475 missense variant C/T snv 0.14 0.11 26
rs8193036 0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 21
rs11362 0.742 0.360 8 6877877 5 prime UTR variant C/T snv 0.43 0.40 13
rs1799946 0.732 0.360 8 6877909 5 prime UTR variant C/T snv 0.36 0.41 13
rs533117495 0.827 0.200 7 87595783 missense variant C/T snv 8.0E-06 5
rs117603931 0.882 0.080 16 2319591 missense variant C/T snv 5.7E-03 6.5E-03 4
rs121434431 0.851 0.080 4 186083346 missense variant C/T snv 4.1E-04 5.2E-04 4
rs28451617 0.851 0.120 7 99735142 5 prime UTR variant C/T snv 9.2E-03 3.3E-02 4