Variant | Gene | N. diseases v | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
17 | 0.724 | 0.400 | 6 | 10404509 | missense variant | T/A;C;G | snv | 4.6E-06 | 0.810 | 1.000 | 3 | 2008 | 2015 | ||||
|
1 | 1.000 | 0.040 | 6 | 10402590 | missense variant | C/T | snv | 0.800 | 1.000 | 1 | 2008 | 2008 | |||||
|
1 | 1.000 | 0.040 | 6 | 10404512 | missense variant | G/A;C | snv | 4.5E-06 | 0.800 | 1.000 | 1 | 2008 | 2008 | ||||
|
2 | 0.925 | 0.120 | 6 | 10402608 | missense variant | G/A | snv | 0.710 | 1.000 | 1 | 2012 | 2012 | |||||
|
9 | 0.851 | 0.080 | 6 | 10404623 | missense variant | G/T | snv | 0.700 | 1.000 | 1 | 2015 | 2015 | |||||
|
7 | 0.807 | 0.120 | 6 | 10404631 | missense variant | A/T | snv | 0.700 | 1.000 | 1 | 2015 | 2015 | |||||
|
3 | 0.925 | 0.040 | 6 | 10404562 | missense variant | C/G;T | snv | 0.700 | 0 | ||||||||
|
3 | 0.925 | 0.040 | 6 | 10404511 | missense variant | C/G;T | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.040 | 6 | 10398417 | stop lost | T/C | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.040 | 6 | 10400584 | missense variant | C/G | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.040 | 6 | 10404523 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.040 | 6 | 10404559 | missense variant | A/G | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.040 | 6 | 10404566 | missense variant | G/A | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.040 | 6 | 10404575 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.040 | 6 | 10409973 | frameshift variant | -/CCGTGCA | delins | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.040 | 6 | 10400587 | missense variant | C/T | snv | 0.700 | 0 |