SLC2A9, solute carrier family 2 member 9, 56606
N. diseases: 74; N. variants: 389
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. | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.882 | 0.160 | 4 | 9993558 | intron variant | G/A;C | snv |
|
0.800 | 1.000 | 8 | 2009 | 2019 | |||||||||
|
0.851 | 0.240 | 4 | 9933120 | intron variant | G/A;T | snv |
|
0.800 | 1.000 | 3 | 2008 | 2016 | |||||||||
|
0.925 | 0.120 | 4 | 9996816 | synonymous variant | C/G;T | snv | 1.2E-05; 0.70 |
|
0.700 | 1.000 | 2 | 2009 | 2011 | ||||||||
|
0.925 | 0.120 | 4 | 9995488 | intron variant | C/A;T | snv |
|
0.700 | 1.000 | 2 | 2009 | 2011 | |||||||||
|
0.851 | 0.240 | 4 | 9921380 | intron variant | G/A;T | snv |
|
0.800 | 1.000 | 2 | 2009 | 2011 | |||||||||
|
0.925 | 0.120 | 4 | 9997711 | intron variant | G/A;T | snv |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.925 | 0.120 | 4 | 9973014 | intron variant | A/G;T | snv |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.925 | 0.120 | 4 | 9885307 | intron variant | A/C;T | snv |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.925 | 0.120 | 4 | 10044203 | intron variant | A/G;T | snv |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.925 | 0.120 | 4 | 9979073 | intron variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.925 | 0.120 | 4 | 10033830 | intron variant | G/A;C | snv |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.925 | 0.120 | 4 | 9901497 | intron variant | A/G;T | snv |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.925 | 0.120 | 4 | 9835466 | intron variant | C/G;T | snv |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.925 | 0.120 | 4 | 10022679 | intron variant | T/A;C | snv |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.925 | 0.120 | 4 | 9971255 | intron variant | T/A;C | snv |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.925 | 0.120 | 4 | 9866793 | intron variant | C/G;T | snv |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.925 | 0.120 | 4 | 9909039 | intron variant | C/A;G | snv |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.925 | 0.120 | 4 | 10042740 | intron variant | T/A;C | snv |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.925 | 0.120 | 4 | 9980567 | intron variant | C/G;T | snv | 0.47 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.925 | 0.120 | 4 | 10038565 | intron variant | C/A;G;T | snv |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.925 | 0.120 | 4 | 9980405 | intron variant | A/G;T | snv |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.925 | 0.120 | 4 | 9980706 | synonymous variant | A/G;T | snv | 0.77; 8.0E-06 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.925 | 0.120 | 4 | 9980265 | intron variant | T/C;G | snv |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.925 | 0.120 | 4 | 10037300 | intron variant | G/A;T | snv |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.925 | 0.120 | 4 | 9816721 | intron variant | T/A;C | snv |
|
0.700 | 1.000 | 1 | 2009 | 2009 |