Variant (rsID / SNP)
rs1126757
rs1126757 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IL11. Location: chromosome 19, position 55,879,872. The table records no clinical significance for this variant.
Reference-table entries
IL11Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 19:55879872
- HGVS
- NM_000641.4,c.246G>A,p.Ala82Ala
- Allele change
- Synonymous_A82A
Associated conditions / phenotypes
Helicobacter Pylori Infection|Endogenous Depression|Mental Depression|Major Depressive Disorder|Gastric Cancer|Depression|Cytokine Deficiency|Thyroid Carcinoma
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.