Variant (rsID / SNP)
rs181206
rs181206 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IL27. Location: chromosome 16, position 28,513,403. The table records no clinical significance for this variant.
Reference-table entries
- Variant type
- missense_variant
- Chromosome / position
- 16:28513403
- HGVS
- NM_145659.3,c.356T>C,p.Leu119Pro
- Allele change
- Missense_L119P
Associated conditions / phenotypes
Esophageal Cancer|Thrombocytopenia Due to Platelet Alloimmunization|Autoimmune Disease|Mycobacterium Tuberculosis 1|Graves' Disease|Hypothyroidism|Systemic Lupus Erythematosus|Bladder Cancer|Pre-Eclampsia|Eclampsia|Allergic Rhinitis|Smoking As a Quantitative Trait Locus 3|Tobacco Addiction|Pulmonary Disease, Chronic Obstructive|Thyroiditis|Thyroid Gland Disease|Rhinitis|Lupus Erythematosus
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.