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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1 | 1.000 | 0.080 | 4 | 105234376 | missense variant | G/A | snv | 5.2E-04 | 2.2E-03 | 0.700 | 0 | ||||||
|
2 | 0.925 | 0.080 | 4 | 105234864 | missense variant | G/A;C | snv | 4.0E-06; 4.0E-06 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.080 | 4 | 105235321 | missense variant | C/T | snv | 1.2E-04 | 1.7E-04 | 0.700 | 0 | ||||||
|
1 | 1.000 | 0.080 | 4 | 105236763 | missense variant | C/T | snv | 1.2E-05 | 2.1E-05 | 0.700 | 0 | ||||||
|
1 | 1.000 | 0.080 | 4 | 105243757 | missense variant | G/A;C | snv | 6.4E-06 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.080 | 4 | 105272630 | missense variant | G/A;T | snv | 3.8E-05; 6.4E-06 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.080 | 4 | 105276128 | missense variant | T/C;G | snv | 1.3E-05 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.080 | 4 | 105276287 | missense variant | G/A | snv | 6.4E-06 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.080 | 4 | 105276331 | missense variant | C/T | snv | 6.4E-06 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.080 | 4 | 105276407 | missense variant | G/A | snv | 5.7E-05 | 1.4E-05 | 0.700 | 0 | ||||||
|
1 | 1.000 | 0.080 | 4 | 105276431 | missense variant | G/T | snv | 0.700 | 0 |