Variant (rsID / SNP)

rs1135824

rs1135824 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP2D6. Location: chromosome 22, position 42,525,044. Clinical significance in the table: Likely benign.

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Reference-table entries

CYP2D6Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 22:42525044
Cytoband: 22q13.2
HGVS: NM_000106.6(CYP2D6):c.496A>G (p.Asn166Asp)
Allele change: Missense_N166D

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.