RAB3GAP2, RAB3 GTPase activating non-catalytic protein subunit 2, 25782
N. diseases: 143; N. variants: 9
Source: ALL
Disease | Type | Disease Class | Semantic Type | N. genes d | N. SNPs d | Score gda | EL gda | EI gda | N. PMIDs | N. SNPs gda | First Ref. | Last Ref. | ||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
disease | Congenital Abnormality | 176 | 23 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 66 | 7 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 130 | 50 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 407 | 35 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 100 | 26 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 71 | 17 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 110 | 13 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 30 | 0.100 | None | 0 | ||||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms | Finding | 45 | 1 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 62 | 0.100 | None | 0 | ||||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases | Finding | 113 | 3 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 30 | 1 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 429 | 29 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 6 | 1 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 22 | 2 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 426 | 39 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 56 | 3 | 0.100 | None | 0 | |||||||||
|
phenotype | Congenital Abnormality | 57 | 3 | 0.100 | None | 0 | |||||||||
|
disease | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases | Congenital Abnormality | 44 | 0.100 | None | 0 | |||||||||
|
phenotype | Pathological Conditions, Signs and Symptoms; Nervous System Diseases | Finding | 30 | 1 | 0.100 | None | 0 | ||||||||
|
phenotype | Nervous System Diseases | Finding | 55 | 5 | 0.100 | None | 0 | ||||||||
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phenotype | Finding | 35 | 3 | 0.100 | None | 0 | |||||||||
|
disease | Congenital Abnormality | 417 | 30 | 0.100 | None | 0 | |||||||||
|
phenotype | Finding | 41 | 1 | 0.100 | None | 0 | |||||||||
|
group | Cardiovascular Diseases | Disease or Syndrome | 925 | 294 | 0.100 | None | 0 |