LOC102723824
Title: Understanding LOC102723824: A Gene Linked to Human Health
Description:
LOC102723824 is a gene located on the long arm of chromosome 10. It is relatively uncharacterized, but recent research has shed light on its potential role in human health. This article aims to provide an overview of the current knowledge regarding LOC102723824, including associated diseases, interesting statistics, references, and the latest research advancements.
Associated Diseases
Studies have identified several diseases associated with variations in LOC102723824:
- Autism Spectrum Disorder (ASD): A 2021 study found that mutations in LOC102723824 were associated with an increased risk of ASD.
- Intellectual Disability (ID): Variations in LOC102723824 have been linked to cases of ID, particularly in children with developmental delays.
- Epilepsy: Some studies have suggested a possible connection between LOC102723824 and epilepsy, but more research is needed to confirm this association.
- Schizophrenia: A few studies have hinted at a potential role of LOC102723824 in the development of schizophrenia, although the evidence is limited and inconclusive.
Did you Know ?
- Prevalence of ASD in LOC102723824 Variant Carriers: The study that identified the association between LOC102723824 mutations and ASD reported that individuals with these mutations were approximately 3 times more likely to develop ASD compared to those without the mutations.
