Variant (rsID / SNP)
rs2295490
rs2295490 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRIB3. Location: chromosome 20, position 368,905. The table records no clinical significance for this variant.
Reference-table entries
- Variant type
- missense_variant
- Chromosome / position
- 20:368905
- HGVS
- NM_001301201.1,c.332A>G,p.Gln111Arg
- Allele change
- Missense_Q84R
Associated conditions / phenotypes
Eye Disease|Vascular Disease|Hypertension, Essential|Prediabetes Syndrome|Type 2 Diabetes Mellitus|Microvascular Complications of Diabetes 6|Microvascular Complications of Diabetes 4|Microvascular Complications of Diabetes 3|Microvascular Complications of Diabetes 7|Lipoprotein Quantitative Trait Locus|Arteries, Anomalies of|Glucose Intolerance
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.