Variant (rsID / SNP)

rs609320

rs609320 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RHCE. Location: chromosome 1, position 25,717,365. Clinical significance in the table: Benign.

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Reference-table entries

RHCEBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:25717365
Cytoband: 1p36.11
HGVS: NM_020485.8(RHCE):c.676= (p.Ala226=)
Allele change: Missense_A226P

Associated conditions / phenotypes

RH E/e 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.