WDR1, WD repeat domain 1, 9948
N. diseases: 59; N. variants: 41
Source: ALL
Variant | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Disease | Disease Class | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.925 | 0.120 | 4 | 10080532 | intron variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.925 | 0.120 | 4 | 10115177 | intron variant | T/C | snv | 0.30 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.925 | 0.120 | 4 | 10096568 | non coding transcript exon variant | G/A;C | snv | 0.44 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.925 | 0.120 | 4 | 10094396 | intron variant | C/T | snv | 0.35 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.925 | 0.120 | 4 | 10073861 | upstream gene variant | C/T | snv | 0.29 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.925 | 0.120 | 4 | 10113899 | intron variant | A/G;T | snv | 0.51 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.925 | 0.120 | 4 | 10105467 | intron variant | C/G | snv | 0.49 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.925 | 0.120 | 4 | 10100969 | intron variant | T/A;C | snv |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.925 | 0.120 | 4 | 10073861 | upstream gene variant | -/AT | delins |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.925 | 0.120 | 4 | 10112281 | intron variant | G/A;C | snv |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.925 | 0.120 | 4 | 10082946 | intron variant | T/G | snv | 0.31 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.925 | 0.120 | 4 | 10084325 | intron variant | G/A | snv | 0.17 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
4 | 10084564 | intron variant | T/G | snv | 0.35 | 0.33 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.925 | 0.120 | 4 | 10088139 | intron variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.925 | 0.120 | 4 | 10098207 | intron variant | A/G | snv | 0.44 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.925 | 0.120 | 4 | 10099459 | intron variant | C/A;G | snv |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.925 | 0.120 | 4 | 10099507 | intron variant | T/C | snv | 0.16 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.925 | 0.120 | 4 | 10104173 | intron variant | T/C | snv | 0.45 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.925 | 0.120 | 4 | 10086371 | intron variant | C/A;G;T | snv |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.925 | 0.120 | 4 | 10082205 | intron variant | C/G | snv | 0.18 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.925 | 0.120 | 4 | 10096352 | non coding transcript exon variant | C/T | snv | 0.16 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.925 | 0.120 | 4 | 10118337 | upstream gene variant | T/C;G | snv |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.925 | 0.120 | 4 | 10093280 | intron variant | T/A;C;G | snv |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.925 | 0.120 | 4 | 10110978 | intron variant | C/G;T | snv |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.925 | 0.120 | 4 | 10113441 | intron variant | T/C | snv | 0.48 |
|
0.700 | 1.000 | 1 | 2009 | 2009 |