Variant (rsID / SNP)
rs7908387
rs7908387 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EIF3A. Location: chromosome 10, position 120,828,969. The table records no clinical significance for this variant.
Reference-table entries
EIF3ANot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 10:120828969
- HGVS
- NM_003750.4,c.939T>C,p.Asp313Asp
- Allele change
- Synonymous_D313D
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.