rs10447760, None

N. diseases: 4
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
0.040 GeneticVariation BEFREE Our study suggested that <i>FOXP2</i> rs10447760 has no effect on the susceptibility to schizophrenia, while it may be associated with its cognitive impairment, especially immediate memory in chronic schizophrenia. 31425145 2019
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
0.040 GeneticVariation BEFREE Thus, our results did not support the association between FOXP2 rs10447760 and schizophrenia in a Chinese Han population, and large-scale genetic replication studies with different racial and geographic origins are required in the future. 29346177 2018
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
0.040 GeneticVariation BEFREE Our findings suggest that the FOXP2 rs10447760 polymorphism may not contribute to the development of schizophrenia, but may contribute to the clinical symptoms of schizophrenia among Han Chinese. 28421313 2017
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
0.040 GeneticVariation BEFREE Our study indicated that the rare variant rs10447760 in FoxP2 may play an important role in schizophrenia and major depression in the Chinese Han population. 22404659 2013