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rs7436338

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs7436338(A;A)
Make rs7436338(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position68567561
GeneUGT2B17
is asnp
is mentioned by
dbSNPrs7436338
ebirs7436338
HLIrs7436338
Exacrs7436338
Varsomers7436338
Maprs7436338
PheGenIrs7436338
hapmaprs7436338
1000 genomesrs7436338
hgdprs7436338
ensemblrs7436338
gopubmedrs7436338
geneviewrs7436338
scholarrs7436338
googlers7436338
pharmgkbrs7436338
gwascentralrs7436338
openSNPrs7436338
23andMers7436338
23andMe allrs7436338
SNP Nexus

SNPshotrs7436338
SNPdbers7436338
MSV3drs7436338
GWAS Ctlgrs7436338
GMAF0.02571
Max Magnitude0
? (A;A) (A;G) (G;G) 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."