Variant (rsID / SNP)
rs179008
rs179008 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TLR7. The table records no clinical significance for this variant.
Reference-table entries
- Variant type
- missense_variant
- HGVS
- NM_016562.4,c.32A>T,p.Gln11Leu
- Allele change
- Missense_Q11L
Associated conditions / phenotypes
Hepatitis C|Hepatitis C Virus|Dengue Hemorrhagic Fever|Dengue Virus|Systemic Lupus Erythematosus|Bronchiolitis|Lupus Erythematosus|Dengue Disease|Sarcoidosis 1|Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity|Dermatitis, Atopic|Pneumonia|Basal Cell Carcinoma|Autoimmune Disease|Skin Carcinoma|Chikungunya|Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant|Ige Responsiveness, Atopic
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.