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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
31 | 0.701 | 0.360 | 15 | 89327201 | missense variant | C/T | snv | 5.1E-04 | 6.7E-04 | 0.810 | 1.000 | 11 | 2003 | 2016 | |||
|
22 | 0.724 | 0.400 | 15 | 89323426 | missense variant | C/G | snv | 9.7E-04 | 7.9E-04 | 0.800 | 1.000 | 10 | 2003 | 2016 | |||
|
4 | 0.925 | 0.160 | 15 | 89325520 | missense variant | G/A | snv | 1.4E-05 | 0.800 | 1.000 | 9 | 2003 | 2006 | ||||
|
3 | 0.882 | 0.200 | 15 | 89320953 | missense variant | G/A | snv | 0.800 | 1.000 | 9 | 2003 | 2006 | |||||
|
2 | 0.925 | 0.200 | 15 | 89319053 | missense variant | C/A;G;T | snv | 3.2E-05; 2.0E-05; 4.0E-06 | 0.800 | 1.000 | 9 | 2003 | 2006 | ||||
|
1 | 1.000 | 0.160 | 15 | 89327006 | missense variant | C/G;T | snv | 1.3E-04; 8.0E-06 | 0.700 | 1.000 | 10 | 2003 | 2016 | ||||
|
3 | 0.882 | 0.200 | 15 | 89326947 | missense variant | C/A;G | snv | 4.8E-03; 2.0E-05 | 0.700 | 1.000 | 9 | 2003 | 2006 | ||||
|
3 | 0.882 | 0.200 | 15 | 89322749 | missense variant | G/A | snv | 2.4E-05 | 1.4E-05 | 0.700 | 1.000 | 9 | 2003 | 2006 | |||
|
1 | 1.000 | 0.160 | 3 | 64099773 | missense variant | C/A | snv | 1.2E-05 | 4.2E-05 | 0.700 | 1.000 | 1 | 2011 | 2011 | |||
|
12 | 0.742 | 0.320 | 15 | 89321792 | missense variant | C/T | snv | 1.5E-04 | 2.7E-04 | 0.700 | 0 | ||||||
|
6 | 0.807 | 0.240 | 15 | 89329055 | missense variant | A/C | snv | 5.7E-05 | 3.5E-05 | 0.700 | 0 | ||||||
|
8 | 0.807 | 0.240 | 15 | 89323460 | missense variant | C/G;T | snv | 6.9E-04; 4.0E-06 | 0.700 | 0 | |||||||
|
6 | 0.807 | 0.240 | 15 | 89321780 | missense variant | G/A | snv | 4.8E-05 | 6.3E-05 | 0.700 | 0 | ||||||
|
6 | 0.807 | 0.240 | 15 | 89318737 | missense variant | G/A;C | snv | 8.0E-06 | 0.700 | 0 | |||||||
|
2 | 0.925 | 0.200 | 15 | 89325519 | missense variant | C/T | snv | 3.2E-05 | 7.7E-05 | 0.700 | 0 |