Variant (rsID / SNP)

rs892586

rs892586 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ELOA2. Location: chromosome 18, position 44,560,429. The table records no clinical significance for this variant.

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Reference-table entries

ELOA2Not classified

Variant type: missense_variant
Chromosome / position: 18:44560429
HGVS: NM_016427.3,c.1207G>T,p.Ala403Ser
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.