Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs28936670 | 0.708 | 0.280 | 5 | 173235011 | missense variant | G/A | snv | 3.4E-03 | 1.1E-02 | 17 | |
rs11008222 | 0.925 | 0.080 | 10 | 30753565 | intergenic variant | G/A | snv | 0.39 | 2 | ||
rs77471149 | 0.925 | 0.080 | 4 | 167914184 | intergenic variant | A/C;G | snv | 2 | |||
rs8061121 | 0.925 | 0.080 | 16 | 87159478 | intron variant | T/C | snv | 0.89 | 2 | ||
rs12045807 | 0.925 | 0.080 | 1 | 150612358 | intron variant | T/C | snv | 0.18 | 2 | ||
rs1642645 | 0.925 | 0.080 | 1 | 42036610 | intron variant | A/C | snv | 0.80 | 2 | ||
rs72820264 | 0.925 | 0.080 | 6 | 9291650 | intron variant | T/C | snv | 0.15 | 2 | ||
rs11894932 | 0.925 | 0.080 | 2 | 98648723 | intron variant | A/C | snv | 0.21 | 2 | ||
rs3746446 | 0.925 | 0.080 | 20 | 34986962 | synonymous variant | T/C | snv | 0.19 | 0.18 | 2 | |
rs55788414 | 0.925 | 0.080 | 16 | 81151334 | intron variant | C/T | snv | 6.3E-02 | 2 | ||
rs1975649 | 0.925 | 0.080 | 3 | 63453210 | intron variant | T/C | snv | 0.74 | 2 |