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 | 0.120 | 17 | 50185789 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 17 | 50185863 | missense variant | A/C | snv | 0.700 | 0 | ||||||||
|
3 | 0.882 | 0.120 | 17 | 50186386 | stop gained | C/A;T | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 17 | 50186493 | missense variant | C/G | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 17 | 50186894 | missense variant | C/A | snv | 0.700 | 1.000 | 20 | 1986 | 2015 | |||||
|
3 | 0.882 | 0.120 | 17 | 50186895 | missense variant | C/T | snv | 0.700 | 1.000 | 20 | 1986 | 2015 | |||||
|
2 | 0.925 | 0.120 | 17 | 50186903 | missense variant | C/A | snv | 0.700 | 1.000 | 20 | 1986 | 2015 | |||||
|
2 | 0.925 | 0.120 | 17 | 50186913 | missense variant | C/T | snv | 0.700 | 1.000 | 20 | 1986 | 2015 | |||||
|
1 | 1.000 | 0.120 | 17 | 50187031 | missense variant | C/T | snv | 0.700 | 1.000 | 20 | 1986 | 2015 | |||||
|
2 | 0.925 | 0.120 | 17 | 50187050 | missense variant | C/A | snv | 0.700 | 1.000 | 20 | 1986 | 2015 | |||||
|
1 | 1.000 | 0.120 | 17 | 50187086 | missense variant | C/G | snv | 0.700 | 1.000 | 20 | 1986 | 2015 | |||||
|
2 | 0.925 | 0.120 | 17 | 50187094 | missense variant | C/A;T | snv | 0.700 | 1.000 | 20 | 1986 | 2015 | |||||
|
1 | 1.000 | 0.120 | 17 | 50187122 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 17 | 50187537 | missense variant | C/A | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 17 | 50187928 | missense variant | C/G | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 17 | 50187946 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 17 | 50187982 | missense variant | C/G | snv | 0.700 | 0 | ||||||||
|
3 | 0.882 | 0.120 | 17 | 50188122 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.120 | 17 | 50188619 | missense variant | C/T | snv | 0.700 | 1.000 | 20 | 1986 | 2015 | |||||
|
2 | 0.925 | 0.120 | 17 | 50188768 | missense variant | C/T | snv | 0.700 | 1.000 | 20 | 1986 | 2015 | |||||
|
2 | 0.925 | 0.120 | 17 | 50188776 | missense variant | C/A;G;T | snv | 0.700 | 1.000 | 20 | 1986 | 2015 | |||||
|
1 | 1.000 | 0.120 | 17 | 50188947 | missense variant | C/A | snv | 0.700 | 1.000 | 20 | 1986 | 2015 | |||||
|
2 | 0.925 | 0.120 | 17 | 50189009 | missense variant | C/A | snv | 0.700 | 1.000 | 20 | 1986 | 2015 | |||||
|
1 | 1.000 | 0.120 | 17 | 50189266 | missense variant | C/A | snv | 0.700 | 1.000 | 20 | 1986 | 2015 | |||||
|
2 | 0.925 | 0.120 | 17 | 50189430 | missense variant | C/A | snv | 0.700 | 1.000 | 20 | 1986 | 2015 |