Variant (rsID / SNP)
rs8027765
rs8027765 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AEN. Location: chromosome 15, position 89,169,858. The table records no clinical significance for this variant.
Reference-table entries
AENNot classified
- Variant type
- missense_variant
- Chromosome / position
- 15:89169858
- HGVS
- NM_022767.4,c.418A>G,p.Asn140Asp
- Allele change
- Missense_N140D
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.