Variant (rsID / SNP)
rs1536928
rs1536928 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR1B1. Location: chromosome 9, position 125,391,409. The table records no clinical significance for this variant.
Reference-table entries
OR1B1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 9:125391409
- HGVS
- NM_001004450.2,c.403T>C,p.Leu135Leu
- Allele change
- Synonymous_L136L
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.