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 | 5 | 1346188 | non coding transcript exon variant | G/C | snv | 0.50 | 0.700 | 1.000 | 1 | 2010 | 2010 | ||||
|
4 | 0.851 | 0.160 | 5 | 1337791 | intron variant | A/T | snv | 0.51 | 0.700 | 1.000 | 1 | 2010 | 2010 | ||||
|
10 | 0.763 | 0.320 | 5 | 1342599 | intron variant | C/A | snv | 0.41 | 0.700 | 1.000 | 1 | 2010 | 2010 | ||||
|
8 | 0.776 | 0.280 | 5 | 1344343 | splice region variant | G/A;T | snv | 0.37; 8.0E-06 | 0.700 | 1.000 | 1 | 2010 | 2010 | ||||
|
8 | 0.776 | 0.200 | 5 | 1320132 | intron variant | G/A | snv | 0.47 | 0.700 | 1.000 | 1 | 2010 | 2010 | ||||
|
42 | 0.620 | 0.640 | 5 | 1321972 | intron variant | C/T | snv | 0.48 | 0.700 | 1.000 | 1 | 2010 | 2010 | ||||
|
2 | 0.925 | 0.160 | 5 | 1320021 | intron variant | G/A | snv | 0.50 | 0.700 | 1.000 | 1 | 2010 | 2010 | ||||
|
5 | 0.827 | 0.200 | 5 | 1319565 | intron variant | C/A;T | snv | 0.700 | 1.000 | 1 | 2010 | 2010 | |||||
|
1 | 1.000 | 0.120 | 5 | 1330725 | non coding transcript exon variant | T/C | snv | 0.46 | 0.700 | 1.000 | 1 | 2010 | 2010 | ||||
|
2 | 0.925 | 0.160 | 5 | 1330138 | intron variant | T/C | snv | 0.46 | 0.700 | 1.000 | 1 | 2010 | 2010 | ||||
|
9 | 0.776 | 0.200 | 5 | 1325688 | non coding transcript exon variant | A/G | snv | 0.46 | 0.700 | 1.000 | 1 | 2010 | 2010 | ||||
|
1 | 1.000 | 0.120 | 5 | 1325652 | non coding transcript exon variant | A/G | snv | 0.46 | 0.700 | 1.000 | 1 | 2010 | 2010 | ||||
|
2 | 0.925 | 0.160 | 5 | 1336106 | intron variant | T/C | snv | 0.50 | 0.700 | 1.000 | 1 | 2010 | 2010 |