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Variant (rsID / SNP)

rs8916

EIF4B

rs8916 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EIF4B. Location: chromosome 12, position 53,433,486. The table records no clinical significance for this variant.

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Reference-table entries

EIF4BNot classified
Variant type
splice_region_variant&synonymous_variant
Chromosome / position
12:53433486
HGVS
NM_001300821.3,c.1770C>T,p.Ser590Ser
Allele change
Synonymous_S590S

Public references

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