Variant (rsID / SNP)
rs1059702
rs1059702 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IRAK1. The table records no clinical significance for this variant.
Reference-table entries
- Variant type
- missense_variant
- HGVS
- NM_001569.4,c.587T>C,p.Phe196Ser
- Allele change
- Missense_F196S
Associated conditions / phenotypes
Systemic Lupus Erythematosus|Lupus Erythematosus|Autoimmune Disease|Scleroderma, Familial Progressive|Rheumatoid Arthritis|Pulmonary Fibrosis|Arthritis|Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity|Graves' Disease|Hashimoto Thyroiditis|Thyroiditis|Neuromyelitis Optica|Lymphomatous Thyroiditis|Systemic Autoimmune Disease|Pleuropneumonia|Fibrosis of Extraocular Muscles, Congenital, 1
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.