Have questions? Visit https://www.reddit.com/r/SNPedia

rs730882251

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730882251(C;T)
Make rs730882251(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome22
GeneCYP2D6
is asnp
is mentioned by
dbSNPrs730882251
ebirs730882251
HLIrs730882251
Exacrs730882251
Varsomers730882251
Maprs730882251
PheGenIrs730882251
hapmaprs730882251
1000 genomesrs730882251
hgdprs730882251
ensemblrs730882251
gopubmedrs730882251
geneviewrs730882251
scholarrs730882251
googlers730882251
pharmgkbrs730882251
gwascentralrs730882251
openSNPrs730882251
23andMers730882251
23andMe allrs730882251
SNP Nexus

SNPshotrs730882251
SNPdbers730882251
MSV3drs730882251
GWAS Ctlgrs730882251
Max Magnitude0
ClinVar
Risk rs730882251(T;T)
Alt rs730882251(T;T)
Reference rs730882251(C;C)
Significance Drug-response
Disease not provided
Variation info
Gene CYP2D6
CLNDBN not provided
Reversed 1
HGVS NC_000022.10:g.42522749G>A
CLNSRC
CLNACC RCV000162079.1,