Rs769258

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Orientationminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs769258(A;A)
Make rs769258(A;G)
ReferenceGRCh37 37.1/131
Chromosome22
Position42526763
GeneCYP2D6
is asnp
is mentioned by
dbSNPrs769258
Exacrs769258
PheGenIrs769258
nextbiors769258
hapmaprs769258
1000 genomesrs769258
hgdprs769258
ensemblrs769258
gopubmedrs769258
geneviewrs769258
scholarrs769258
googlers769258
pharmgkbrs769258
gwascentralrs769258
openSNPrs769258
23andMers769258
23andMe allrs769258
SNP Nexus

SNPshotrs769258
SNPdbers769258
MSV3drs769258
GMAF0.02755
Max Magnitude0
? (A;A) (A;G) (G;G) 28
a variation in CYP2D6

[PMID 20070850OA-icon.png] Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. [PMID 23133420OA-icon.png] Pharmacogenomic Diversity among Brazilians: Influence of Ancestry, Self-Reported Color, and Geographical Origin.