FAM3C, FAM3 metabolism regulating signaling molecule C, 10447
N. diseases: 32; N. variants: 13
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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
7 | 121378803 | intron variant | A/T | snv | 0.31 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
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7 | 121378525 | intron variant | C/A;T | snv | 0.33 |
|
0.700 | 1.000 | 2 | 2012 | 2017 | ||||||||||
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7 | 121378525 | intron variant | C/A;T | snv | 0.33 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
1.000 | 0.080 | 7 | 121393067 | intron variant | T/C | snv | 0.28 |
|
0.700 | 1.000 | 2 | 2009 | 2014 | ||||||||
|
7 | 121390854 | intron variant | GGGGGGGGGGGGGGGG/-;G;GG;GGG;GGGG;GGGGG;GGGGGG;GGGGGGG;GGGGGGGG;GGGGGGGGG;GGGGGGGGGG;GGGGGGGGGGG;GGGGGGGGGGGG;GGGGGGGGGGGGG;GGGGGGGGGGGGGG;GGGGGGGGGGGGGGG;GGGGGGGGGGGGGGGGG;GGGGGGGGGGGGGGGGGG;GGGGGGGGGGGGGGGGGGG | delins | 5.6E-03 |
|
0.700 | 1.000 | 1 | 2014 | 2014 | ||||||||||
|
7 | 121390853 | intron variant | C/G;T | snv |
|
0.700 | 1.000 | 1 | 2014 | 2014 | |||||||||||
|
7 | 121390854 | intron variant | GGGGGGGGGGGGGGGG/-;G;GG;GGG;GGGG;GGGGG;GGGGGG;GGGGGGG;GGGGGGGG;GGGGGGGGG;GGGGGGGGGG;GGGGGGGGGGG;GGGGGGGGGGGG;GGGGGGGGGGGGG;GGGGGGGGGGGGGG;GGGGGGGGGGGGGGG;GGGGGGGGGGGGGGGGG;GGGGGGGGGGGGGGGGGG;GGGGGGGGGGGGGGGGGGG | delins | 5.8E-02 |
|
0.700 | 1.000 | 1 | 2014 | 2014 | ||||||||||
|
7 | 121390854 | intron variant | GGGGGGGGGGGGGGGG/-;G;GG;GGG;GGGG;GGGGG;GGGGGG;GGGGGGG;GGGGGGGG;GGGGGGGGG;GGGGGGGGGG;GGGGGGGGGGG;GGGGGGGGGGGG;GGGGGGGGGGGGG;GGGGGGGGGGGGGG;GGGGGGGGGGGGGGG;GGGGGGGGGGGGGGGGG;GGGGGGGGGGGGGGGGGG;GGGGGGGGGGGGGGGGGGG | delins | 5.9E-04 |
|
0.700 | 1.000 | 1 | 2014 | 2014 | ||||||||||
|
7 | 121367195 | intron variant | T/C | snv | 0.56 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
7 | 121354619 | intron variant | T/C | snv | 0.55 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
7 | 121350783 | intron variant | C/G | snv | 0.52 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
7 | 121358223 | intron variant | T/A;G | snv |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||||
|
7 | 121391825 | intron variant | C/T | snv | 0.53 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
7 | 121385448 | intron variant | T/C | snv | 0.29 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1.000 | 0.080 | 7 | 121393067 | intron variant | T/C | snv | 0.28 |
|
Nutritional and Metabolic Diseases; Musculoskeletal Diseases | 0.010 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 7 | 121393067 | intron variant | T/C | snv | 0.28 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
7 | 121378803 | intron variant | A/T | snv | 0.31 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
7 | 121378525 | intron variant | C/A;T | snv | 0.33 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1.000 | 0.080 | 7 | 121393067 | intron variant | T/C | snv | 0.28 |
|
0.700 | 1.000 | 1 | 2009 | 2009 |