Variant (rsID / SNP)
rs2228467
rs2228467 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACKR2. Location: chromosome 3, position 42,906,116. The table records no clinical significance for this variant.
Reference-table entries
ACKR2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 3:42906116
- HGVS
- NM_001296.5,c.122T>C,p.Val41Ala
- Allele change
- Missense_V41A
Associated conditions / phenotypes
Alzheimer Disease
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.