Variant (rsID / SNP)
rs1051922
rs1051922 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IFNB1. Location: chromosome 9, position 21,077,716. The table records no clinical significance for this variant.
Reference-table entries
IFNB1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 9:21077716
- HGVS
- NM_002176.4,c.153C>T,p.Tyr51Tyr
- Allele change
- Synonymous_Y51Y
Associated conditions / phenotypes
Malaria
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.