Variant (rsID / SNP)
rs78014467
rs78014467 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ELOA2. Location: chromosome 18, position 44,559,730. The table records no clinical significance for this variant.
Reference-table entries
ELOA2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 18:44559730
- HGVS
- NM_016427.3,c.1906G>A,p.Gly636Ser
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.