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 | |||||||||
|
0.925 | 0.120 | 4 | 9925343 | intron variant | T/G | snv | 0.39 |
|
0.800 | 1.000 | 6 | 2009 | 2018 | ||||||||
|
0.827 | 0.200 | 4 | 9920543 | missense variant | C/T | snv | 0.24 | 0.29 |
|
0.800 | 1.000 | 5 | 2008 | 2016 | |||||||
|
0.851 | 0.160 | 4 | 9914117 | intron variant | C/T | snv | 0.32 |
|
0.800 | 1.000 | 4 | 2009 | 2019 | ||||||||
|
0.827 | 0.240 | 4 | 9992591 | intron variant | C/T | snv | 0.82 |
|
0.800 | 1.000 | 4 | 2009 | 2017 | ||||||||
|
0.882 | 0.200 | 4 | 9995266 | intron variant | T/C | snv | 0.82 |
|
0.800 | 1.000 | 3 | 2009 | 2018 | ||||||||
|
0.851 | 0.240 | 4 | 9933120 | intron variant | G/A;T | snv |
|
0.800 | 1.000 | 3 | 2008 | 2016 | |||||||||
|
0.925 | 0.120 | 4 | 9964756 | intron variant | A/G | snv | 0.28 |
|
0.800 | 1.000 | 3 | 2008 | 2009 | ||||||||
|
0.925 | 0.120 | 4 | 9918723 | intron variant | T/C | snv | 0.51 |
|
0.800 | 1.000 | 2 | 2009 | 2015 | ||||||||
|
0.925 | 0.120 | 4 | 9942428 | intron variant | A/G | snv | 0.33 |
|
0.800 | 1.000 | 2 | 2009 | 2013 | ||||||||
|
0.925 | 0.120 | 4 | 9987609 | intron variant | C/T | snv | 0.84 |
|
0.800 | 1.000 | 2 | 2009 | 2018 | ||||||||
|
0.925 | 0.120 | 4 | 9922695 | intron variant | A/G | snv | 0.70 |
|
0.800 | 1.000 | 2 | 2009 | 2013 | ||||||||
|
0.851 | 0.200 | 4 | 9934286 | intron variant | A/G | snv | 0.33 |
|
0.800 | 1.000 | 2 | 2007 | 2009 | ||||||||
|
0.851 | 0.240 | 4 | 9921380 | intron variant | G/A;T | snv |
|
0.800 | 1.000 | 2 | 2009 | 2011 | |||||||||
|
0.925 | 0.120 | 4 | 10054752 | intron variant | T/C | snv | 0.73 |
|
0.800 | 1.000 | 2 | 2009 | 2011 | ||||||||
|
0.925 | 0.120 | 4 | 9939810 | intron variant | C/T | snv | 0.39 |
|
0.800 | 1.000 | 2 | 2009 | 2019 | ||||||||
|
0.925 | 0.120 | 4 | 9983972 | intron variant | G/A | snv | 0.80 |
|
0.800 | 1.000 | 2 | 2009 | 2015 | ||||||||
|
4 | 9983752 | intron variant | G/T | snv | 0.65 |
|
0.700 | 1.000 | 3 | 2018 | 2019 | ||||||||||
|
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 | 9996869 | synonymous variant | A/G | snv | 0.80 | 0.79 |
|
0.700 | 1.000 | 2 | 2009 | 2011 | |||||||
|
0.925 | 0.120 | 4 | 9995679 | non coding transcript exon variant | G/A | snv | 0.72 |
|
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 | |||||||||
|
0.925 | 0.120 | 4 | 9992214 | intron variant | C/G;T | snv | 0.71 |
|
0.700 | 1.000 | 2 | 2009 | 2011 | ||||||||
|
0.925 | 0.120 | 4 | 9957651 | intron variant | C/T | snv | 0.48 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.925 | 0.120 | 4 | 9982851 | intron variant | C/T | snv | 0.21 |
|
0.700 | 1.000 | 1 | 2009 | 2009 |