Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4906902 | 0.724 | 0.200 | 15 | 26774621 | intron variant | A/G | snv | 0.15 | 14 | ||
rs211037 | 0.742 | 0.240 | 5 | 162101274 | synonymous variant | C/T | snv | 0.28 | 0.31 | 14 | |
rs121909673 | 0.776 | 0.080 | 5 | 162093965 | missense variant | G/A | snv | 10 | |||
rs121909674 | 0.790 | 0.080 | 5 | 162153132 | stop gained | C/T | snv | 8 | |||
rs25409 | 0.882 | 0.080 | 15 | 26773694 | missense variant | G/A | snv | 2.9E-03 | 3.5E-03 | 4 | |
rs267606697 | 0.925 | 0.040 | 16 | 1204325 | missense variant | G/A | snv | 2.4E-04 | 4.2E-05 | 3 | |
rs41292285 | 1.000 | 0.040 | 16 | 1208033 | missense variant | G/T | snv | 7.3E-03 | 7.1E-03 | 3 | |
rs540638287 | 1.000 | 0.040 | 16 | 1204313 | missense variant | C/T | snv | 4.3E-05 | 1.4E-05 | 3 | |
rs8044363 | 0.925 | 0.040 | 16 | 1200559 | synonymous variant | T/A;C | snv | 0.37 | 3 | ||
rs1570624 | 0.882 | 0.040 | 6 | 52454252 | missense variant | G/A | snv | 1.0E-02 | 9.6E-03 | 3 | |
rs373363000 | 0.882 | 0.080 | 5 | 161686327 | missense variant | C/A;T | snv | 4.0E-06; 3.3E-04 | 3 | ||
rs71651682 | 0.925 | 0.040 | 15 | 26772759 | missense variant | C/T | snv | 3 | |||
rs9934839 | 0.925 | 0.040 | 16 | 1202259 | synonymous variant | A/G | snv | 0.42 | 0.50 | 2 | |
rs10462087 | 0.925 | 0.040 | 5 | 45295178 | intron variant | T/C | snv | 5.5E-02 | 2 | ||
rs1053074 | 0.925 | 0.040 | 1 | 160039331 | 3 prime UTR variant | A/C | snv | 0.46 | 2 | ||
rs12729701 | 0.925 | 0.040 | 1 | 160042616 | intron variant | A/G | snv | 0.19 | 2 | ||
rs371775791 | 0.925 | 0.040 | 15 | 22866495 | missense variant | A/G | snv | 7.2E-05 | 5.6E-05 | 2 |