LOC101929095
Loc101929095: A Comprehensive Exploration
Description:
Loc101929095 is a genetic variant located on chromosome 10. It is a single nucleotide polymorphism (SNP), meaning it represents a variation in a single base pair of DNA. The reference allele for this SNP is guanine (G), while the alternative allele is cytosine (C).
Associated Diseases:
Loc101929095 has been associated with several diseases, including:
- Systemic lupus erythematosus (SLE): SLE is an autoimmune disease that affects connective tissues throughout the body. Loc101929095 is a known risk factor for developing SLE, with individuals carrying the C allele having an increased susceptibility.
- Multiple sclerosis (MS): MS is a chronic neurological disorder that affects the central nervous system. Loc101929095 has been linked to an increased risk of MS, particularly among individuals of European descent.
- Type 1 diabetes: Type 1 diabetes is an autoimmune disease that affects the pancreas and insulin production. Loc101929095 has been associated with an increased risk of developing type 1 diabetes, especially in younger individuals.
Did you Know ?
In a study involving over 10,000 individuals, researchers found that those who carried the C allele of Loc101929095 had a 20% increased risk of developing SLE compared to individuals who carried the G allele.
