Variant (rsID / SNP)

rs3812448

rs3812448 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EEF1D. Location: chromosome 8, position 144,671,922. The table records no clinical significance for this variant.

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Reference-table entries

EEF1DNot classified

Variant type: synonymous_variant
Chromosome / position: 8:144671922
HGVS: NM_001130053.5,c.330C>T,p.Arg110Arg
Allele change: Silent

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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