Variant (rsID / SNP)
rs5092
rs5092 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to APOA4. Location: chromosome 11, position 116,693,464. The table records no clinical significance for this variant.
Reference-table entries
APOA4Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 11:116693464
- HGVS
- NM_000482.4,c.87G>A,p.Thr29Thr
- Allele change
- Synonymous_T29T
Associated conditions / phenotypes
Mental Depression|Major Depressive Disorder|Depression
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.