Variant (rsID / SNP)
rs17841292
rs17841292 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EEF2K. Location: chromosome 16, position 22,237,273. The table records no clinical significance for this variant.
Reference-table entries
EEF2KNot classified
- Variant type
- missense_variant
- Chromosome / position
- 16:22237273
- HGVS
- NM_013302.5,c.223C>G,p.Pro75Ala
- Allele change
- Missense_P75A
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.