MIR6886, microRNA 6886, 102465534
N. diseases: 6; N. variants: 286
Source: ALL
Variant | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Disease | Disease Class | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.925 | 0.080 | 19 | 11113308 | missense variant | G/A;C | snv | 1.6E-05 |
|
0.700 | 0 | |||||||||||
|
0.827 | 0.200 | 19 | 11113337 | missense variant | C/T | snv | 2.4E-05 | 7.0E-06 |
|
0.700 | 0 | ||||||||||
|
0.925 | 0.080 | 19 | 11113414 | missense variant | C/G;T | snv | 3.2E-04 |
|
0.700 | 0 | |||||||||||
|
0.925 | 0.080 | 19 | 11111586 | missense variant | A/C | snv | 8.0E-06 |
|
0.700 | 0 | |||||||||||
|
0.827 | 0.120 | 19 | 11113590 | missense variant | G/A;T | snv | 5.6E-05 | 2.1E-05 |
|
0.700 | 0 | ||||||||||
|
0.882 | 0.080 | 19 | 11113752 | missense variant | C/A;T | snv | 8.0E-06 |
|
0.700 | 0 | |||||||||||
|
0.925 | 0.080 | 19 | 11113392 | missense variant | C/A;G;T | snv | 4.0E-06; 8.0E-06 |
|
0.700 | 0 | |||||||||||
|
0.925 | 0.080 | 19 | 11113705 | missense variant | C/T | snv | 1.6E-05 |
|
0.700 | 0 | |||||||||||
|
0.851 | 0.160 | 19 | 11111514 | missense variant | A/C;G;T | snv | 4.0E-06 |
|
0.700 | 0 | |||||||||||
|
1.000 | 0.080 | 19 | 11113678 | missense variant | C/A;T | snv | 8.0E-06 |
|
0.700 | 0 | |||||||||||
|
0.882 | 0.160 | 19 | 11111519 | missense variant | G/A;C;T | snv | 1.2E-05 |
|
0.700 | 0 | |||||||||||
|
0.925 | 0.080 | 19 | 11111556 | missense variant | G/A;C | snv | 1.2E-05 |
|
0.700 | 0 | |||||||||||
|
0.882 | 0.160 | 19 | 11113338 | missense variant | G/A;C;T | snv | 1.6E-05 |
|
0.700 | 0 | |||||||||||
|
1.000 | 0.080 | 19 | 11113312 | missense variant | C/A;T | snv | 2.0E-05 |
|
0.700 | 0 | |||||||||||
|
0.925 | 0.080 | 19 | 11111522 | missense variant | G/A;C | snv |
|
0.700 | 0 | ||||||||||||
|
0.882 | 0.160 | 19 | 11111544 | missense variant | G/A;C;T | snv |
|
0.700 | 0 | ||||||||||||
|
0.925 | 0.080 | 19 | 11111555 | missense variant | T/C;G | snv | 4.0E-06 |
|
0.700 | 0 | |||||||||||
|
0.925 | 0.080 | 19 | 11111570 | missense variant | G/A;T | snv | 4.0E-06 |
|
0.700 | 0 | |||||||||||
|
0.925 | 0.080 | 19 | 11111571 | missense variant | G/A;C;T | snv |
|
0.700 | 0 | ||||||||||||
|
0.925 | 0.080 | 19 | 11111577 | missense variant | A/C;G | snv |
|
0.700 | 0 | ||||||||||||
|
0.925 | 0.080 | 19 | 11111627 | missense variant | T/C | snv |
|
0.700 | 0 | ||||||||||||
|
0.925 | 0.080 | 19 | 11113306 | missense variant | C/G;T | snv |
|
0.700 | 0 | ||||||||||||
|
0.827 | 0.120 | 19 | 11113314 | missense variant | A/C;T | snv |
|
0.700 | 0 | ||||||||||||
|
1.000 | 0.080 | 19 | 11113334 | missense variant | G/C | snv |
|
0.700 | 0 | ||||||||||||
|
0.925 | 0.080 | 19 | 11113346 | missense variant | T/C;G | snv |
|
0.700 | 0 |