Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs34778348 | 0.742 | 0.120 | 12 | 40363526 | missense variant | G/A | snv | 1.7E-03 | 5.8E-04 | 1 | |
rs34637584 | 0.583 | 0.480 | 12 | 40340400 | missense variant | G/A | snv | 5.3E-04 | 3.6E-04 | 1 | |
rs11175593 | 0.882 | 0.160 | 12 | 40208138 | non coding transcript exon variant | C/T | snv | 2.8E-02 | 3 | ||
rs11564273 | 1.000 | 0.040 | 12 | 40204350 | intron variant | T/G | snv | 6.5E-02 | 1 | ||
rs28903073 | 1.000 | 0.040 | 12 | 40259708 | intron variant | G/A | snv | 2.4E-03 | 1 | ||
rs1491942 | 1.000 | 0.040 | 12 | 40227006 | intron variant | C/G | snv | 0.23 | 1 |