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Variant (rsID / SNP)

rs9935059

EEF2K

rs9935059 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EEF2K. Location: chromosome 16, position 22,237,118. The table records no clinical significance for this variant.

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Reference-table entries

EEF2KNot classified
Variant type
missense_variant
Chromosome / position
16:22237118
HGVS
NM_013302.5,c.68A>G,p.His23Arg
Allele change
Missense_H23R

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.