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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
6 | 0.827 | 0.280 | 4 | 10000237 | intron variant | G/A | snv | 0.72 | 0.700 | 1.000 | 1 | 2009 | 2009 | ||||
|
3 | 0.925 | 0.120 | 4 | 10000801 | intron variant | T/C | snv | 0.24 | 0.700 | 1.000 | 1 | 2009 | 2009 | ||||
|
3 | 0.925 | 0.120 | 4 | 10001041 | intron variant | T/A;C | snv | 0.700 | 1.000 | 1 | 2009 | 2009 | |||||
|
3 | 0.925 | 0.120 | 4 | 10001771 | intron variant | C/G | snv | 0.46 | 0.700 | 1.000 | 1 | 2009 | 2009 | ||||
|
3 | 0.925 | 0.120 | 4 | 10003119 | intron variant | C/G | snv | 0.43 | 0.700 | 1.000 | 1 | 2009 | 2009 | ||||
|
3 | 0.925 | 0.120 | 4 | 10003208 | intron variant | A/G | snv | 0.72 | 0.700 | 1.000 | 1 | 2009 | 2009 | ||||
|
3 | 0.925 | 0.120 | 4 | 10003811 | intron variant | G/A | snv | 0.72 | 0.700 | 1.000 | 1 | 2009 | 2009 | ||||
|
3 | 0.925 | 0.120 | 4 | 10004913 | intron variant | C/A | snv | 0.72 | 0.700 | 1.000 | 1 | 2009 | 2009 | ||||
|
3 | 0.925 | 0.120 | 4 | 10005462 | intron variant | C/T | snv | 0.72 | 0.700 | 1.000 | 1 | 2009 | 2009 | ||||
|
3 | 0.925 | 0.120 | 4 | 10005651 | intron variant | C/G;T | snv | 0.700 | 1.000 | 1 | 2009 | 2009 | |||||
|
3 | 0.925 | 0.120 | 4 | 10006681 | non coding transcript exon variant | G/A;C | snv | 0.700 | 1.000 | 1 | 2009 | 2009 | |||||
|
3 | 0.925 | 0.120 | 4 | 10011549 | intron variant | T/G | snv | 0.55 | 0.700 | 1.000 | 1 | 2009 | 2009 | ||||
|
3 | 0.925 | 0.120 | 4 | 10011839 | intron variant | T/A;G | snv | 0.700 | 1.000 | 1 | 2009 | 2009 | |||||
|
3 | 0.925 | 0.120 | 4 | 10016529 | intron variant | C/A;G;T | snv | 0.700 | 1.000 | 1 | 2009 | 2009 | |||||
|
3 | 0.925 | 0.120 | 4 | 10018108 | intron variant | C/T | snv | 0.44 | 0.700 | 1.000 | 1 | 2009 | 2009 | ||||
|
3 | 0.925 | 0.120 | 4 | 10018856 | intron variant | C/T | snv | 0.44 | 0.700 | 1.000 | 1 | 2009 | 2009 | ||||
|
3 | 0.925 | 0.120 | 4 | 10018940 | intron variant | G/A | snv | 0.52 | 0.44 | 0.700 | 1.000 | 1 | 2009 | 2009 | |||
|
3 | 0.925 | 0.120 | 4 | 10019666 | intron variant | G/C | snv | 0.44 | 0.700 | 1.000 | 1 | 2009 | 2009 | ||||
|
3 | 0.925 | 0.120 | 4 | 10019971 | intron variant | C/G;T | snv | 0.700 | 1.000 | 1 | 2009 | 2009 | |||||
|
1 | 4 | 100200234 | intron variant | A/G;T | snv | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
1 | 4 | 10021983 | intron variant | C/T | snv | 3.1E-03 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||
|
3 | 0.925 | 0.120 | 4 | 10022679 | intron variant | T/A;C | snv | 0.700 | 1.000 | 1 | 2009 | 2009 | |||||
|
3 | 0.925 | 0.120 | 4 | 10023539 | intron variant | T/A | snv | 0.54 | 0.700 | 1.000 | 1 | 2009 | 2009 | ||||
|
1 | 4 | 10027243 | intron variant | G/A | snv | 0.22 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||
|
3 | 0.925 | 0.120 | 4 | 10029170 | non coding transcript exon variant | G/C | snv | 0.79 | 0.700 | 1.000 | 1 | 2009 | 2009 |