Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs941576 | 1.000 | 0.120 | 14 | 100839708 | intron variant | A/G | snv | 0.45 | 1 | ||
rs917997 | 0.701 | 0.480 | 2 | 102454108 | downstream gene variant | T/A;C | snv | 6 | |||
rs34536443 | 0.667 | 0.400 | 19 | 10352442 | missense variant | G/C | snv | 2.7E-02 | 2.8E-02 | 4 | |
rs12720356 | 0.752 | 0.360 | 19 | 10359299 | missense variant | A/C;G | snv | 6.1E-02; 4.0E-06 | 2 | ||
rs2304256 | 0.732 | 0.360 | 19 | 10364976 | missense variant | C/A | snv | 0.27 | 0.23 | 3 | |
rs9810233 | 0.925 | 0.200 | 3 | 105292046 | intergenic variant | A/G | snv | 0.25 | 1 | ||
rs1358030 | 0.925 | 0.120 | 10 | 106363841 | intergenic variant | G/A | snv | 0.57 | 1 | ||
rs12931878 | 1.000 | 0.120 | 16 | 10948337 | intron variant | A/G | snv | 0.14 | 1 | ||
rs12923849 | 1.000 | 0.120 | 16 | 10968140 | intron variant | G/A | snv | 0.13 | 1 | ||
rs17229044 | 1.000 | 0.120 | 16 | 10969079 | intron variant | C/T | snv | 0.16 | 1 | ||
rs13330041 | 1.000 | 0.120 | 16 | 10994951 | intron variant | G/A | snv | 0.25 | 2 | ||
rs725613 | 0.851 | 0.240 | 16 | 11075826 | intron variant | T/G | snv | 0.42 | 2 | ||
rs2041670 | 0.851 | 0.280 | 16 | 11080795 | intron variant | G/A;C | snv | 2 | |||
rs7200786 | 0.882 | 0.200 | 16 | 11083944 | intron variant | A/G | snv | 0.59 | 2 | ||
rs12708716 | 0.807 | 0.320 | 16 | 11086016 | intron variant | A/G | snv | 0.37 | 4 | ||
rs886125 | 1.000 | 0.120 | 12 | 110927520 | intergenic variant | A/G | snv | 0.57 | 1 | ||
rs12924729 | 0.882 | 0.200 | 16 | 11093926 | intron variant | G/A | snv | 0.34 | 2 | ||
rs12599402 | 0.925 | 0.160 | 16 | 11096031 | intron variant | T/C | snv | 0.51 | 2 | ||
rs12927355 | 0.882 | 0.240 | 16 | 11100914 | intron variant | C/A;T | snv | 0.29 | 2 | ||
rs998592 | 0.925 | 0.160 | 16 | 11105821 | intron variant | C/T | snv | 0.39 | 1 | ||
rs9933507 | 1.000 | 0.120 | 16 | 11107571 | intron variant | T/C | snv | 0.46 | 1 | ||
rs1265564 | 1.000 | 0.120 | 12 | 111270654 | non coding transcript exon variant | A/C | snv | 0.30 | 1 | ||
rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 24 | ||
rs2903692 | 0.807 | 0.360 | 16 | 11144926 | intron variant | G/A | snv | 0.33 | 1 | ||
rs17673553 | 1.000 | 0.120 | 16 | 11148049 | intron variant | A/G | snv | 0.18 | 2 |