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 | 19 | 18786040 | missense variant | C/A | snv | 0.810 | 1.000 | 13 | 1995 | 2012 | |||||
|
1 | 1.000 | 0.080 | 19 | 18785789 | missense variant | C/T | snv | 4.0E-06 | 0.700 | 1.000 | 12 | 1995 | 2012 | ||||
|
1 | 1.000 | 0.080 | 19 | 18786051 | missense variant | C/T | snv | 0.800 | 1.000 | 12 | 1995 | 2012 | |||||
|
1 | 1.000 | 0.080 | 19 | 18787644 | missense variant | A/G | snv | 0.800 | 1.000 | 12 | 1995 | 2012 | |||||
|
1 | 1.000 | 0.080 | 19 | 18787584 | missense variant | A/G | snv | 0.800 | 1.000 | 12 | 1995 | 2012 | |||||
|
1 | 1.000 | 0.080 | 19 | 18788654 | missense variant | G/A | snv | 2.4E-04 | 2.4E-04 | 0.700 | 1.000 | 12 | 1995 | 2012 | |||
|
1 | 1.000 | 0.080 | 19 | 18787572 | missense variant | G/A;C | snv | 2.8E-05; 4.0E-06 | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||
|
1 | 1.000 | 0.080 | 19 | 18785050 | missense variant | T/C | snv | 0.710 | 1.000 | 1 | 2004 | 2004 | |||||
|
1 | 1.000 | 0.080 | 19 | 18786036 | missense variant | T/C | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.080 | 19 | 18785063 | missense variant | C/G;T | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.080 | 19 | 18785056 | missense variant | G/A;C;T | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.080 | 19 | 18785755 | missense variant | G/A | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.080 | 19 | 18783126 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.080 | 19 | 18783125 | missense variant | C/T | snv | 0.810 | 1.000 | 13 | 1995 | 2012 | |||||
|
2 | 0.925 | 0.080 | 19 | 18787500 | missense variant | C/A | snv | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.080 | 19 | 18786035 | inframe insertion | TCG/-;TCGTCG;TCGTCGTCG | delins | 0.700 | 0 |