Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs699 | 0.501 | 0.800 | 1 | 230710048 | missense variant | A/G | snv | 0.55 | 0.58 | 134 | |
rs1137101 | 0.554 | 0.760 | 1 | 65592830 | missense variant | A/G | snv | 0.51 | 0.50 | 77 | |
rs4762 | 0.637 | 0.440 | 1 | 230710231 | missense variant | G/A | snv | 0.12 | 0.11 | 35 | |
rs1061622 | 0.633 | 0.760 | 1 | 12192898 | missense variant | T/G | snv | 0.22 | 0.22 | 33 | |
rs629301 | 0.851 | 0.120 | 1 | 109275684 | 3 prime UTR variant | G/T | snv | 0.74 | 22 | ||
rs5068 | 0.776 | 0.160 | 1 | 11845917 | 3 prime UTR variant | A/G;T | snv | 13 | |||
rs3766871 | 0.790 | 0.240 | 1 | 237614784 | missense variant | G/A;T | snv | 4.0E-02 | 9 | ||
rs57045855 | 0.882 | 0.040 | 1 | 156134464 | missense variant | A/G;T | snv | 6 | |||
rs61195471 | 0.827 | 0.160 | 1 | 156134496 | missense variant | G/A | snv | 6 | |||
rs12564445 | 0.851 | 0.040 | 1 | 201376359 | intron variant | G/A | snv | 0.27 | 5 | ||
rs567798234 | 0.851 | 0.120 | 1 | 109625326 | missense variant | C/T | snv | 4.1E-06 | 7.0E-06 | 5 | |
rs121918598 | 0.851 | 0.080 | 1 | 237648523 | missense variant | G/A;C | snv | 4 | |||
rs1739843 | 0.882 | 0.040 | 1 | 16016759 | intron variant | T/C | snv | 0.62 | 4 | ||
rs198358 | 0.925 | 0.040 | 1 | 11844019 | 3 prime UTR variant | T/C | snv | 0.32 | 4 | ||
rs61661343 | 0.851 | 0.040 | 1 | 156130687 | missense variant | T/C | snv | 4 | |||
rs10927887 | 0.925 | 0.040 | 1 | 16024780 | missense variant | A/C;G | snv | 0.55 | 3 | ||
rs1253810269 | 0.882 | 0.080 | 1 | 26696971 | missense variant | G/A | snv | 7.0E-06 | 3 | ||
rs188344082 | 1.000 | 0.040 | 1 | 18783262 | intergenic variant | G/A | snv | 1.8E-02 | 3 | ||
rs61823501 | 1.000 | 0.040 | 1 | 184396836 | intron variant | C/T | snv | 0.12 | 3 | ||
rs74056623 | 1.000 | 0.040 | 1 | 18784584 | intergenic variant | G/A | snv | 8.3E-02 | 3 | ||
rs74056624 | 1.000 | 0.040 | 1 | 18790006 | intergenic variant | G/A | snv | 2.3E-02 | 3 | ||
rs749303395 | 0.882 | 0.040 | 1 | 114680329 | missense variant | G/A;C | snv | 8.0E-06; 4.0E-06 | 3 | ||
rs780094 | 0.658 | 0.400 | 2 | 27518370 | intron variant | T/C | snv | 0.67 | 62 | ||
rs562338 | 0.807 | 0.160 | 2 | 21065449 | intergenic variant | A/G | snv | 0.69 | 21 | ||
rs1728918 | 0.827 | 0.160 | 2 | 27412596 | upstream gene variant | A/G;T | snv | 19 |