Variant (rsID / SNP)
rs3811047
rs3811047 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IL37. Location: chromosome 2, position 113,671,410. Clinical significance in the table: Benign.
Reference-table entries
- Clinical significance (as recorded)
- Benign
- Variant type
- missense_variant
- Chromosome / position
- 2:113671410
- HGVS
- NM_014439.4,c.124A>G,p.Thr42Ala
- Allele change
- Missense_T42A
Associated conditions / phenotypes
Rheumatoid Arthritis|Autoimmune Disease|Adenocarcinoma|Arthritis|Lipoprotein Quantitative Trait Locus|Arteries, Anomalies of|Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets|Peptic Ulcer Disease|Gastrointestinal System Disease|Inflammatory Spondylopathy|Spondyloarthropathy 1|Spondylitis|Graves' Disease|Thyroiditis|Exanthem|Proteinuria, Chronic Benign|Systemic Lupus Erythematosus|Open-Angle Glaucoma
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.