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rs28371733

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 1.5 Homozygous for CYP2D6*52 variant.
(A;G) 1 Carrier of one CYP2D6*52 variant.
(C;C) 3 Homozygous for non-functioning CYP2D6*4H variant.
(C;G) 2 Carrier of one CYP2D6*4H non-functioning variant.
(G;G) 0 normal
ReferenceGRCh37 37.1/131
Chromosome22
Position42522916
GeneCYP2D6
is asnp
is mentioned by
dbSNPrs28371733
ebirs28371733
HLIrs28371733
Exacrs28371733
Varsomers28371733
Maprs28371733
PheGenIrs28371733
hapmaprs28371733
1000 genomesrs28371733
hgdprs28371733
ensemblrs28371733
gopubmedrs28371733
geneviewrs28371733
scholarrs28371733
googlers28371733
pharmgkbrs28371733
gwascentralrs28371733
openSNPrs28371733
23andMers28371733
23andMe allrs28371733
SNP Nexus

SNPshotrs28371733
SNPdbers28371733
MSV3drs28371733
GWAS Ctlgrs28371733
Max Magnitude3
The wild type allele for this SNP is (G) in minus orientation. When it changes to (C) it is known as 3877G>C and is a marker for non-functioning variant CYP2D6*4H.

When it changes to (A) it is known as 3877G>A and is a marker for variant CYP2D6*52 which is possibly a decreased functioning variant, though more study is needed.[PMID 19364831]

Please note that this is in minus orientation and the 3877G>C version is subject to ambiguous flip.