Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs374528680 | 0.851 | 0.240 | 12 | 2686216 | missense variant | G/A;C | snv | 4.0E-06; 6.0E-05 | 5 | ||
rs587782933 | 0.827 | 0.200 | 12 | 2504526 | missense variant | G/A | snv | 5 | |||
rs61752115 | 0.807 | 0.320 | 2 | 61048535 | missense variant | T/C | snv | 4.0E-06 | 7 | ||
rs730880056 | 1.000 | 0.200 | 12 | 2593261 | missense variant | G/A;C | snv | 1.2E-05 | 1 | ||
rs786205745 | 0.807 | 0.320 | 12 | 2504538 | missense variant | G/A;C | snv | 6 | |||
rs794727587 | 1.000 | 0.200 | 12 | 2665600 | missense variant | C/G | snv | 1 | |||
rs797044881 | 1.000 | 0.200 | 12 | 2608651 | missense variant | T/C | snv | 1 | |||
rs79891110 | 0.807 | 0.320 | 12 | 2504944 | stop gained | G/A;T | snv | 6 | |||
rs80315385 | 0.882 | 0.200 | 12 | 2504932 | missense variant | G/A | snv | 3 |