Variant (rsID / SNP)
rs3811046
rs3811046 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IL37. Location: chromosome 2, position 113,671,378. The table records no clinical significance for this variant.
Reference-table entries
IL37Not classified
- Variant type
- missense_variant
- Chromosome / position
- 2:113671378
- HGVS
- NM_014439.4,c.92G>T,p.Gly31Val
- Allele change
- Missense_G31V
Associated conditions / phenotypes
Periodontitis|Graves' Disease|Aggressive Periodontitis|Periodontitis, Chronic|Thyroiditis|Open-Angle Glaucoma|Rheumatoid Arthritis|Glaucoma, Primary Open Angle|Intraocular Pressure Quantitative Trait Locus|Arthritis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.