SLC25A44, solute carrier family 25 member 44, 9673
N. diseases: 4; N. variants: 19
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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1 | 156195499 | intron variant | T/G | snv | 0.42 |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2014 | 2014 | |||||||||
|
1 | 156195526 | intron variant | G/C | snv | 0.42 |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2014 | 2014 | |||||||||
|
1.000 | 0.040 | 1 | 156211979 | 3 prime UTR variant | A/G | snv | 0.43 |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2014 | 2014 | |||||||
|
1 | 156195551 | intron variant | T/A;G | snv |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2014 | 2014 | ||||||||||
|
1 | 156198945 | non coding transcript exon variant | T/C | snv | 0.43 |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2014 | 2014 | |||||||||
|
1 | 156192768 | upstream gene variant | A/G | snv | 0.42 |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2014 | 2014 | |||||||||
|
1 | 156204684 | intron variant | T/C | snv | 0.42 |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2014 | 2014 | |||||||||
|
1 | 156195094 | intron variant | C/G | snv | 0.30 |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2014 | 2014 | |||||||||
|
1 | 156203894 | intron variant | T/C | snv | 0.42 |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2014 | 2014 | |||||||||
|
1 | 156202334 | intron variant | T/C;G | snv | 0.43 |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2014 | 2014 | |||||||||
|
1.000 | 0.040 | 1 | 156201505 | intron variant | C/G | snv | 0.42 |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2014 | 2014 | |||||||
|
1 | 156211216 | 3 prime UTR variant | C/G | snv | 0.43 |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2014 | 2014 | |||||||||
|
1.000 | 0.040 | 1 | 156212919 | upstream gene variant | T/C;G | snv |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
1.000 | 0.120 | 1 | 156199819 | non coding transcript exon variant | A/G | snv | 0.34 | 0.43 |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2014 | 2014 |