| Variant | Gene | Disease | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
0.710 | GeneticVariation | UNIPROT | |||||||||||
|
|
T | 0.700 | GeneticVariation | CLINVAR | ||||||||||
|
|
C | 0.700 | GeneticVariation | CLINVAR | ||||||||||
|
|
0.700 | GeneticVariation | UNIPROT | |||||||||||
|
|
0.700 | GeneticVariation | UNIPROT | |||||||||||
|
|
0.700 | GeneticVariation | UNIPROT | |||||||||||
|
|
T | 0.700 | GeneticVariation | CLINVAR | ||||||||||
|
|
ATC | 0.700 | CausalMutation | CLINVAR | ||||||||||
|
|
C | 0.700 | GeneticVariation | CLINVAR | ||||||||||
|
|
C | 0.700 | CausalMutation | CLINVAR | ||||||||||
|
|
0.700 | GeneticVariation | UNIPROT | Mutations of the Nogo-66 receptor (RTN4R) gene in schizophrenia. | 15532024 | 2004 |
||||||||
|
|
0.700 | GeneticVariation | UNIPROT | Mutations of the Nogo-66 receptor (RTN4R) gene in schizophrenia. | 15532024 | 2004 |
||||||||
|
|
0.700 | GeneticVariation | UNIPROT | Mutations of the Nogo-66 receptor (RTN4R) gene in schizophrenia. | 15532024 | 2004 |
||||||||
|
|
C | 0.710 | GeneticVariation | GWASCAT | We report results of a case-control WGA study in schizophrenia, examining approximately 500 000 markers, which revealed a strong effect (P=3.7 x 10(-7)) of a novel locus (rs4129148) near the CSF2RA (colony stimulating factor, receptor 2 alpha) gene in the pseudoautosomal region. | 17522711 | 2007 |
|||||||
|
|
G | 0.860 | GeneticVariation | GWASDB | Genome-wide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in women. | 18282107 | 2008 |
|||||||
|
|
G | 0.860 | GeneticVariation | GWASCAT | Genome-wide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in women. | 18282107 | 2008 |
|||||||
|
|
A | 0.800 | GeneticVariation | GWASDB | A genome-wide association study in 574 schizophrenia trios using DNA pooling. | 18332876 | 2009 |
|||||||
|
|
A | 0.800 | GeneticVariation | GWASCAT | A genome-wide association study in 574 schizophrenia trios using DNA pooling. | 18332876 | 2009 |
|||||||
|
|
T | 0.900 | GeneticVariation | GWASDB | Identification of loci associated with schizophrenia by genome-wide association and follow-up. | 18677311 | 2008 |
|||||||
|
|
T | 0.900 | GeneticVariation | GWASCAT | Identification of loci associated with schizophrenia by genome-wide association and follow-up. | 18677311 | 2008 |
|||||||
|
|
0.700 | GeneticVariation | GWASCAT | A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype. | 19023125 | 2009 |
||||||||
|
|
0.700 | GeneticVariation | UNIPROT | Genetic variants of Nogo-66 receptor with possible association to schizophrenia block myelin inhibition of axon growth. | 19052207 | 2008 |
||||||||
|
|
0.700 | GeneticVariation | UNIPROT | Genetic variants of Nogo-66 receptor with possible association to schizophrenia block myelin inhibition of axon growth. | 19052207 | 2008 |
||||||||
|
|
0.700 | GeneticVariation | UNIPROT | Genetic variants of Nogo-66 receptor with possible association to schizophrenia block myelin inhibition of axon growth. | 19052207 | 2008 |
||||||||
|
|
C | 0.700 | CausalMutation | CLINVAR | SPG11 mutations cause Kjellin syndrome, a hereditary spastic paraplegia with thin corpus callosum and central retinal degeneration. | 19194956 | 2009 |