MICAL3, microtubule associated monooxygenase, calponin and LIM domain containing 3, 57553
N. diseases: 17; N. variants: 12
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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
22 | 17957192 | intron variant | C/T | snv | 0.21 |
|
0.800 | 1.000 | 1 | 2011 | 2011 | ||||||||||
|
22 | 17967521 | intron variant | A/T | snv | 0.20 |
|
0.700 | 1.000 | 2 | 2015 | 2017 | ||||||||||
|
22 | 17999834 | intron variant | G/A | snv | 0.20 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
22 | 17965347 | intron variant | C/T | snv | 0.17 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
22 | 17965347 | intron variant | C/T | snv | 0.17 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
22 | 17965347 | intron variant | C/T | snv | 0.17 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
22 | 17803906 | intron variant | T/C | snv | 0.39 | 0.52 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
1.000 | 0.120 | 22 | 17833538 | intron variant | C/T | snv | 0.30 |
|
Digestive System Diseases; Neoplasms; Endocrine System Diseases | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
22 | 17951228 | intron variant | G/T | snv | 0.26 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
22 | 17842301 | non coding transcript exon variant | A/G | snv | 0.51 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
22 | 17985603 | intron variant | A/C | snv | 0.34 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
1.000 | 0.040 | 22 | 18006117 | non coding transcript exon variant | G/C | snv | 0.19 |
|
Respiratory Tract Diseases | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
22 | 17935399 | intron variant | C/T | snv | 0.19 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
0.925 | 0.040 | 22 | 17816431 | intron variant | A/G | snv | 0.33 |
|
Musculoskeletal Diseases | 0.010 | < 0.001 | 1 | 2012 | 2012 | |||||||
|
0.925 | 0.040 | 22 | 17816431 | intron variant | A/G | snv | 0.33 |
|
Musculoskeletal Diseases | 0.010 | < 0.001 | 1 | 2012 | 2012 |