FAM13A, family with sequence similarity 13 member A, 10144
N. diseases: 64; N. variants: 66
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 | 0.040 | 4 | 88962828 | intron variant | C/T | snv | 0.53 |
|
Respiratory Tract Diseases | 0.840 | 1.000 | 6 | 2010 | 2015 | |||||||
|
0.827 | 0.120 | 4 | 88948181 | intron variant | T/C | snv | 0.49 |
|
Respiratory Tract Diseases | 0.820 | 0.750 | 4 | 2010 | 2015 | |||||||
|
0.925 | 0.080 | 4 | 88965146 | intron variant | C/G;T | snv |
|
Respiratory Tract Diseases | 0.710 | 1.000 | 3 | 2010 | 2015 | ||||||||
|
4 | 88808923 | intron variant | C/T | snv | 0.50 |
|
0.700 | 1.000 | 3 | 2018 | 2019 | ||||||||||
|
4 | 88820118 | intron variant | G/A;C | snv |
|
0.800 | 1.000 | 3 | 2013 | 2018 | |||||||||||
|
4 | 88831125 | intron variant | G/A | snv | 0.22 |
|
0.700 | 1.000 | 3 | 2017 | 2019 | ||||||||||
|
1.000 | 0.040 | 4 | 88947927 | intron variant | C/T | snv | 0.47 |
|
Respiratory Tract Diseases | 0.700 | 1.000 | 2 | 2014 | 2019 | |||||||
|
0.827 | 0.120 | 4 | 88948181 | intron variant | T/C | snv | 0.49 |
|
0.800 | 1.000 | 2 | 2012 | 2015 | ||||||||
|
0.827 | 0.120 | 4 | 88948181 | intron variant | T/C | snv | 0.49 |
|
0.700 | 1.000 | 2 | 2010 | 2012 | ||||||||
|
0.925 | 0.080 | 4 | 88945562 | intron variant | T/C | snv | 0.45 |
|
Respiratory Tract Diseases | 0.700 | 1.000 | 2 | 2014 | 2014 | |||||||
|
4 | 89007052 | intron variant | T/C | snv | 0.54 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||||
|
4 | 89007052 | intron variant | T/C | snv | 0.54 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||||
|
4 | 88911381 | intron variant | C/T | snv | 0.28 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||||
|
4 | 88911381 | intron variant | C/T | snv | 0.28 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||||
|
4 | 88829210 | intron variant | A/G | snv | 0.37 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||||
|
4 | 88829210 | intron variant | A/G | snv | 0.37 |
|
0.700 | 1.000 | 1 | 2010 | 2010 | ||||||||||
|
4 | 88829210 | intron variant | A/G | snv | 0.37 |
|
0.700 | 1.000 | 1 | 2010 | 2010 | ||||||||||
|
4 | 88829210 | intron variant | A/G | snv | 0.37 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||||
|
4 | 88919909 | intron variant | C/T | snv | 0.29 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||||
|
4 | 88919909 | intron variant | C/T | snv | 0.29 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||||
|
4 | 88920019 | intron variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2015 | 2015 | |||||||||||
|
0.882 | 0.160 | 4 | 88726273 | 3 prime UTR variant | T/A | snv | 0.46 |
|
Neoplasms; Skin and Connective Tissue Diseases | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.882 | 0.160 | 4 | 88726273 | 3 prime UTR variant | T/A | snv | 0.46 |
|
Neoplasms; Skin and Connective Tissue Diseases | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.882 | 0.160 | 4 | 88726273 | 3 prime UTR variant | T/A | snv | 0.46 |
|
Pathological Conditions, Signs and Symptoms; Digestive System Diseases | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
4 | 88878055 | intron variant | C/T | snv | 0.29 |
|
0.700 | 1.000 | 1 | 2015 | 2015 |