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 | 22 | 32043363 | missense variant | G/A | snv | 0.810 | 1.000 | 5 | 1991 | 2001 | |||||
|
1 | 1.000 | 0.120 | 22 | 32066992 | missense variant | G/A | snv | 0.010 | 1.000 | 1 | 2018 | 2018 | |||||
|
1 | 1.000 | 0.120 | 22 | 32084539 | missense variant | C/G | snv | 0.010 | 1.000 | 1 | 2018 | 2018 | |||||
|
1 | 1.000 | 0.120 | 22 | 32084966 | missense variant | G/A | snv | 4.0E-06 | 0.710 | 1.000 | 4 | 1991 | 2001 | ||||
|
1 | 1.000 | 0.120 | 22 | 32099305 | missense variant | C/A;T | snv | 2.0E-05; 4.0E-06 | 0.710 | 1.000 | 1 | 1999 | 1999 | ||||
|
1 | 1.000 | 0.120 | 22 | 32091618 | missense variant | G/A | snv | 8.0E-06; 4.0E-06 | 2.1E-05 | 0.010 | 1.000 | 1 | 2018 | 2018 | |||
|
1 | 1.000 | 0.120 | 22 | 32043364 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 0.800 | 1.000 | 4 | 1991 | 2001 | |||
|
2 | 1.000 | 0.120 | 22 | 32110063 | missense variant | C/G;T | snv | 4.8E-02; 2.4E-05 | 0.010 | 1.000 | 1 | 2011 | 2011 | ||||
|
1 | 1.000 | 0.120 | 22 | 32104793 | missense variant | G/A | snv | 4.4E-05 | 1.4E-05 | 0.710 | 1.000 | 1 | 2011 | 2011 | |||
|
3 | 1.000 | 0.120 | 22 | 32049959 | missense variant | A/G | snv | 4.8E-02 | 4.5E-02 | 0.010 | 1.000 | 1 | 2011 | 2011 | |||
|
2 | 1.000 | 0.120 | 22 | 32091713 | missense variant | G/A | snv | 4.9E-02 | 4.5E-02 | 0.010 | 1.000 | 1 | 2011 | 2011 | |||
|
65 | 0.578 | 0.640 | 8 | 37966280 | missense variant | A/G | snv | 0.11 | 9.2E-02 | 0.010 | < 0.001 | 1 | 2004 | 2004 |