Variant (rsID / SNP)

rs5030867

rs5030867 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP2D6. Location: chromosome 22, position 42,523,858. Clinical significance in the table: Likely benign; other.

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Reference-table entries

CYP2D6Likely benign

Clinical significance (as recorded): Likely benign; other
Variant type: single nucleotide variant
Chromosome / position: 22:42523858
Cytoband: 22q13.2
HGVS: NM_000106.5(CYP2D6):c.971A>C (p.His324Pro)
Allele change: Missense_H324P

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.