Variant (rsID / SNP)
rs3213545
rs3213545 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OASL. Location: chromosome 12, position 121,471,337. The table records no clinical significance for this variant.
Reference-table entries
OASLNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 12:121471337
- HGVS
- NM_003733.4,c.408C>T,p.Leu136Leu
- Allele change
- Synonymous_L136L
Associated conditions / phenotypes
Hepatitis C|West Nile Virus|West Nile Virus Infection|Viral Infectious Disease
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.