Variant (rsID / SNP)
rs4459610
rs4459610 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACE3P. Location: chromosome 17, position 61,584,720. The table records no clinical significance for this variant.
Reference-table entries
ACE3PNot classified
- Variant type
- intragenic_variant
- Chromosome / position
- 17:61584720
- HGVS
- ACE3P,n.61584720A>T
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.