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Variant (rsID / SNP)

rs9466

EIF3L

rs9466 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EIF3L. Location: chromosome 22, position 38,273,749. The table records no clinical significance for this variant.

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Reference-table entries

EIF3LNot classified
Variant type
synonymous_variant
Chromosome / position
22:38273749
HGVS
NM_016091.4,c.1146T>C,p.Ile382Ile
Allele change
Synonymous_I382I

Public references

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