Variant (rsID / SNP)
rs273259
rs273259 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IFI44L. Location: chromosome 1, position 79,093,818. The table records no clinical significance for this variant.
Reference-table entries
IFI44LNot classified
- Variant type
- missense_variant
- Chromosome / position
- 1:79093818
- HGVS
- NM_001375646.1,c.218A>G,p.His73Arg
- Allele change
- Missense_H73R
Associated conditions / phenotypes
Otitis Media|Measles|Febrile Seizures|Mumps|Rubella|Seizure Disorder
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.