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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
2 | 1.000 | 0.080 | 4 | 38829975 | intron variant | G/A | snv | 0.62 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||
|
2 | 1.000 | 0.080 | 4 | 38852748 | intron variant | C/T | snv | 0.29 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||
|
1 | 4 | 38857718 | upstream gene variant | C/T | snv | 0.14 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||
|
1 | 4 | 38831586 | intron variant | C/A;G | snv | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||||
|
1 | 4 | 38831106 | intron variant | C/T | snv | 0.14 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||
|
21 | 0.689 | 0.360 | 4 | 38828729 | missense variant | A/G | snv | 0.73 | 0.72 | 0.700 | 1.000 | 1 | 2013 | 2013 | |||
|
1 | 4 | 38845390 | intron variant | T/C | snv | 0.62 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||
|
1 | 4 | 38846296 | intron variant | T/A;C | snv | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||||
|
1 | 4 | 38842128 | intron variant | G/A;C | snv | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||||
|
1 | 4 | 38843577 | intron variant | G/A | snv | 0.39 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||
|
1 | 4 | 38854763 | intron variant | G/A | snv | 0.59 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||
|
1 | 4 | 38845358 | intron variant | C/G;T | snv | 0.700 | 1.000 | 1 | 2013 | 2013 |