Variant (rsID / SNP)

rs2814778

rs2814778 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACKR1. Location: chromosome 1, position 159,174,683. Clinical significance in the table: Pathogenic; association; protective.

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Reference-table entries

ACKR1Pathogenic

Clinical significance (as recorded): Pathogenic; association; protective
Variant type: single nucleotide variant
Chromosome / position: 1:159174683
Cytoband: 1q23.2
HGVS: NM_002036.3(ACKR1):c.-67T>C
Allele change: Silent

Associated conditions / phenotypes

DUFFY BLOOD GROUP SYSTEM, FY(a-b-) PHENOTYPE|White blood cell count quantitative trait locus 1|Plasmodium vivax, resistance to

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.