Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3775439 | 1.000 | 0.040 | 4 | 89788590 | intron variant | G/A | snv | 0.25 | 1 | ||
rs3796661 | 1.000 | 0.040 | 4 | 89766356 | intron variant | C/T | snv | 8.7E-02 | 1 | ||
rs3822086 | 1.000 | 0.040 | 4 | 89743643 | intron variant | C/T | snv | 0.24 | 1 | ||
rs3857053 | 1.000 | 0.040 | 4 | 89724523 | 3 prime UTR variant | C/T | snv | 0.24 | 1 | ||
rs3857059 | 1.000 | 0.040 | 4 | 89754087 | intron variant | A/G;T | snv | 1 | |||
rs7684318 | 1.000 | 0.040 | 4 | 89733852 | intron variant | T/C | snv | 0.19 | 1 | ||
rs894278 | 0.882 | 0.080 | 4 | 89813384 | intron variant | T/G | snv | 0.15 | 1 |