Variant (rsID / SNP)

rs905450

rs905450 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EFL1. Location: chromosome 15, position 82,444,437. The table records no clinical significance for this variant.

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Reference-table entries

EFL1Not classified

Variant type: synonymous_variant
Chromosome / position: 15:82444437
HGVS: NM_001322845.2,c.2358T>C,p.Gly786Gly
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.