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rs13327941

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs13327941(A;A)
Make rs13327941(A;C)
ReferenceGRCh38 38.1/141
Chromosome4
Position68556427
GeneUGT2B17
is asnp
is mentioned by
dbSNPrs13327941
ebirs13327941
HLIrs13327941
Exacrs13327941
Varsomers13327941
Maprs13327941
PheGenIrs13327941
hapmaprs13327941
1000 genomesrs13327941
hgdprs13327941
ensemblrs13327941
gopubmedrs13327941
geneviewrs13327941
scholarrs13327941
googlers13327941
pharmgkbrs13327941
gwascentralrs13327941
openSNPrs13327941
23andMers13327941
23andMe allrs13327941
SNP Nexus

SNPshotrs13327941
SNPdbers13327941
MSV3drs13327941
GWAS Ctlgrs13327941
GMAF0.005051
Max Magnitude0
? (A;A) (A;C) (C;C) 28
[PMID 18334593] Deletion of both copies of this gene alters testosterone metabolism making steroid use undetectable.

The first page of this thesis claims that the deletion allele has a frequency of 4.8% in Swedes but is completely absent in Koreans. While its abstract claims "it is a common polymorphism with an allele frequency of 29 % in Swedes and 78 % in Koreans."