Variant (rsID / SNP)
rs4325604
rs4325604 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR1A1. Location: chromosome 17, position 3,119,008. The table records no clinical significance for this variant.
Reference-table entries
OR1A1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 17:3119008
- HGVS
- NM_001386104.1,c.94T>C,p.Leu32Leu
- Allele change
- Synonymous_L32L
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
