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rs10025771

From SNPedia

Orientationplus
Stabilizedplus
Make rs10025771(C;C)
Make rs10025771(C;T)
Make rs10025771(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position68539507
GeneUGT2B17
is asnp
is mentioned by
dbSNPrs10025771
ebirs10025771
HLIrs10025771
Exacrs10025771
Varsomers10025771
Maprs10025771
PheGenIrs10025771
hapmaprs10025771
1000 genomesrs10025771
hgdprs10025771
ensemblrs10025771
gopubmedrs10025771
geneviewrs10025771
scholarrs10025771
googlers10025771
pharmgkbrs10025771
gwascentralrs10025771
openSNPrs10025771
23andMers10025771
23andMe allrs10025771
SNP Nexus

SNPshotrs10025771
SNPdbers10025771
MSV3drs10025771
GWAS Ctlgrs10025771
GMAF0.4986
Max Magnitude
? (C;C) (C;T) (T;T) 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."