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 | 3 | 37025752 | missense variant | G/A;C;T | snv | 5.2E-05 | 0.700 | 1.000 | 35 | 1996 | 2017 | ||||
|
1 | 1.000 | 0.080 | 3 | 37050634 | missense variant | A/G | snv | 7.6E-05 | 3.5E-05 | 0.700 | 1.000 | 20 | 1996 | 2012 | |||
|
1 | 1.000 | 0.080 | 3 | 37025977 | missense variant | A/C | snv | 1.6E-04 | 7.0E-05 | 0.700 | 1.000 | 20 | 1996 | 2012 | |||
|
1 | 1.000 | 0.080 | 3 | 37050534 | missense variant | C/T | snv | 5.6E-03 | 2.3E-02 | 0.700 | 1.000 | 20 | 1996 | 2012 | |||
|
1 | 1.000 | 0.080 | 3 | 37048587 | missense variant | T/C | snv | 0.700 | 1.000 | 20 | 1996 | 2012 | |||||
|
1 | 1.000 | 0.080 | 3 | 37048910 | missense variant | T/C | snv | 0.700 | 1.000 | 20 | 1996 | 2012 | |||||
|
1 | 1.000 | 0.080 | 3 | 36993599 | missense variant | C/G;T | snv | 4.0E-06; 3.2E-05 | 0.700 | 1.000 | 20 | 1996 | 2012 | ||||
|
1 | 1.000 | 0.080 | 3 | 37004420 | missense variant | A/C;G | snv | 0.700 | 1.000 | 20 | 1996 | 2012 | |||||
|
1 | 1.000 | 0.080 | 3 | 37004425 | missense variant | G/C | snv | 0.700 | 1.000 | 20 | 1996 | 2012 | |||||
|
1 | 1.000 | 0.080 | 3 | 37025763 | missense variant | C/A;G;T | snv | 4.0E-06 | 0.700 | 1.000 | 20 | 1996 | 2012 | ||||
|
1 | 1.000 | 0.080 | 3 | 36993638 | missense variant | GC/TG | mnv | 0.700 | 1.000 | 20 | 1996 | 2012 | |||||
|
1 | 1.000 | 0.080 | 3 | 37011827 | missense variant | G/A;C | snv | 4.0E-06 | 0.700 | 1.000 | 20 | 1996 | 2012 | ||||
|
1 | 1.000 | 0.080 | 3 | 37042293 | missense variant | A/T | snv | 8.0E-06 | 0.700 | 1.000 | 20 | 1996 | 2012 | ||||
|
1 | 1.000 | 0.080 | 3 | 37047679 | missense variant | A/C;G | snv | 0.700 | 1.000 | 20 | 1996 | 2012 | |||||
|
1 | 1.000 | 0.080 | 3 | 37040279 | missense variant | A/C;G | snv | 8.0E-06 | 0.700 | 1.000 | 20 | 1996 | 2012 | ||||
|
1 | 1.000 | 0.080 | 3 | 37020387 | missense variant | G/A;T | snv | 4.0E-06 | 0.700 | 1.000 | 20 | 1996 | 2012 | ||||
|
1 | 1.000 | 0.080 | 3 | 37040273 | missense variant | T/C | snv | 0.700 | 1.000 | 20 | 1996 | 2012 | |||||
|
1 | 1.000 | 0.080 | 3 | 37028827 | missense variant | G/C;T | snv | 0.700 | 1.000 | 20 | 1996 | 2012 | |||||
|
1 | 1.000 | 0.080 | 3 | 37017560 | missense variant | C/G | snv | 7.0E-06 | 0.700 | 1.000 | 20 | 1996 | 2012 | ||||
|
1 | 1.000 | 0.080 | 3 | 37025919 | missense variant | G/A | snv | 3.4E-04 | 3.3E-04 | 0.700 | 1.000 | 20 | 1996 | 2012 | |||
|
1 | 1.000 | 0.080 | 3 | 37017590 | missense variant | T/C | snv | 0.700 | 1.000 | 20 | 1996 | 2012 | |||||
|
1 | 1.000 | 0.080 | 3 | 37014532 | missense variant | C/G;T | snv | 4.0E-06 | 0.700 | 1.000 | 20 | 1996 | 2012 | ||||
|
1 | 1.000 | 0.080 | 3 | 37014455 | missense variant | A/G | snv | 0.700 | 1.000 | 20 | 1996 | 2012 | |||||
|
1 | 1.000 | 0.080 | 3 | 36996708 | missense variant | G/A;C | snv | 0.700 | 1.000 | 20 | 1996 | 2012 | |||||
|
1 | 1.000 | 0.080 | 3 | 37025751 | missense variant | C/T | snv | 6.0E-05 | 4.9E-05 | 0.700 | 1.000 | 15 | 2001 | 2017 |