rs28371733

Orientation

minus

Stabilized

minus

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

Reference

GRCh37 37.1/131

Chromosome

22

Position

42126914

Gene	CYP2D6, LOC102723722

is a	snp
is	mentioned by
dbSNP	rs28371733
dbSNP (classic)	rs28371733
ClinGen	rs28371733
ebi	rs28371733
HLI	rs28371733
Exac	rs28371733
Gnomad	rs28371733
Varsome	rs28371733
LitVar	rs28371733
Map	rs28371733
PheGenI	rs28371733
Biobank	rs28371733
1000 genomes	rs28371733
hgdp	rs28371733
ensembl	rs28371733
geneview	rs28371733
scholar	rs28371733
google	rs28371733
pharmgkb	rs28371733
gwascentral	rs28371733
openSNP	rs28371733
23andMe	rs28371733
SNPshot	rs28371733
SNPdbe	rs28371733
MSV3d	rs28371733
GWAS Ctlg	rs28371733

Max Magnitude

3

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.