Variant (rsID / SNP)

rs12075

rs12075 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACKR1. Location: chromosome 1, position 159,175,354. Clinical significance in the table: Benign.

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Reference-table entries

ACKR1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:159175354
Cytoband: 1q23.2
HGVS: NM_002036.4(ACKR1):c.125G>A (p.Gly42Asp)
Allele change: Missense_G42D

Associated conditions / phenotypes

DUFFY BLOOD GROUP SYSTEM, FYA/FYB POLYMORPHISM

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.