Variant (rsID / SNP)

rs2229593

rs2229593 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACKR2. Location: chromosome 3, position 42,906,216. The table records no clinical significance for this variant.

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Reference-table entries

ACKR2Not classified

Variant type: synonymous_variant
Chromosome / position: 3:42906216
HGVS: NM_001296.5,c.222C>T,p.Tyr74Tyr
Allele change: Synonymous_Y74Y

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.