Variant (rsID / SNP)

rs116871238

rs116871238 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EFL1. Location: chromosome 15, position 82,512,118. The table records no clinical significance for this variant.

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Reference-table entries

EFL1Not classified

Variant type: missense_variant
Chromosome / position: 15:82512118
HGVS: NM_001322845.2,c.1486C>T,p.Leu496Phe
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.