Variant:
rs5030865 at chr22:42525035 in CYP2D6

Alleles (on + chromosomal strand)
C > G
C > T
Amino Acid Translation
Gly169Xaa

Variant Annotations

PharmGKB variant annotations provide information about variant-drug pairs based on individual PubMed publications. Each annotation represents information from a single paper and the goal is to report the information that the author states, not an interpretation of the paper. The PMID for supporting PubMed publications is found in the "Evidence" field.

Information presented, including study size, allele frequencies and statistics is taken directly from the publication. However, if the author does not correct p-values in cases of multiple hypotheses, curators may apply a Bonferroni correction. Curators attempt to report study size based on the actual number of participants used for the calculation of the association statistics, so the number may vary slightly from what is reported in the abstract of the paper. OMB Race Category information is derived from the paper and mapped to standardized categories. Category definitions may be found by clicking on the "OMB Race Category" link.

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Publications related to rs5030865 at chr22:42525035: 1

No Dosing Guideline available No Drug Label available No Clinical Annotation available VA No VIP available No VIP available
Frequency of CYP2D6*10 and *14 alleles and their influence on the metabolic activity of CYP2D6 in a healthy Chinese population. Clinical pharmacology and therapeutics. 2007. Cai W M, et al. [Article:17186005@PubMed]

Cross-References

UCSC Golden Path:
chr22:42525035
dbSNP:
rs5030865

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