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rs11723091

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs11723091(G;G)
Make rs11723091(G;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position68539752
GeneUGT2B17
is asnp
is mentioned by
dbSNPrs11723091
ebirs11723091
HLIrs11723091
Exacrs11723091
Varsomers11723091
Maprs11723091
PheGenIrs11723091
hapmaprs11723091
1000 genomesrs11723091
hgdprs11723091
ensemblrs11723091
gopubmedrs11723091
geneviewrs11723091
scholarrs11723091
googlers11723091
pharmgkbrs11723091
gwascentralrs11723091
openSNPrs11723091
23andMers11723091
23andMe allrs11723091
SNP Nexus

SNPshotrs11723091
SNPdbers11723091
MSV3drs11723091
GWAS Ctlgrs11723091
Max Magnitude0
[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."