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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
5 | 0.851 | 0.080 | 2 | 165998049 | missense variant | G/T | snv | 0.800 | 1.000 | 4 | 2005 | 2009 | |||||
|
5 | 0.851 | 0.120 | 2 | 165996099 | missense variant | A/G | snv | 7.0E-06 | 0.800 | 1.000 | 4 | 2005 | 2009 | ||||
|
1 | 1.000 | 0.040 | 2 | 165998047 | missense variant | C/G | snv | 0.800 | 1.000 | 4 | 2005 | 2009 | |||||
|
14 | 0.752 | 0.120 | 2 | 166015636 | missense variant | G/C | snv | 1.7E-03 | 1.6E-03 | 0.700 | 1.000 | 4 | 2005 | 2009 | |||
|
4 | 0.851 | 0.080 | 2 | 166073371 | missense variant | T/C | snv | 0.700 | 0 | ||||||||
|
3 | 0.882 | 0.080 | 2 | 165992341 | missense variant | C/G;T | snv | 0.700 | 0 | ||||||||
|
8 | 0.790 | 0.080 | 2 | 166052869 | missense variant | G/A;C | snv | 0.700 | 0 | ||||||||
|
5 | 0.827 | 0.080 | 2 | 166052882 | stop gained | G/A | snv | 0.700 | 0 | ||||||||
|
3 | 0.882 | 0.080 | 2 | 165996047 | stop gained | G/A;C;T | snv | 2.0E-05 | 0.700 | 0 | |||||||
|
4 | 0.851 | 0.080 | 2 | 166043875 | stop gained | G/A;T | snv | 4.0E-06 | 0.700 | 0 | |||||||
|
4 | 0.851 | 0.080 | 2 | 166037930 | missense variant | C/G;T | snv | 0.700 | 0 | ||||||||
|
6 | 0.827 | 0.120 | 2 | 166054637 | splice donor variant | C/A;G;T | snv | 0.700 | 0 | ||||||||
|
3 | 0.882 | 0.080 | 2 | 166044010 | stop gained | G/A | snv | 0.700 | 0 | ||||||||
|
3 | 0.882 | 0.080 | 2 | 166052885 | missense variant | G/C | snv | 1.4E-05 | 0.700 | 0 |