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rs7435827

From SNPedia

Orientationplus
Stabilizedplus
Make rs7435827(A;A)
Make rs7435827(A;G)
Make rs7435827(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position68549226
GeneUGT2B17
is asnp
is mentioned by
dbSNPrs7435827
ebirs7435827
HLIrs7435827
Exacrs7435827
Varsomers7435827
Maprs7435827
PheGenIrs7435827
hapmaprs7435827
1000 genomesrs7435827
hgdprs7435827
ensemblrs7435827
gopubmedrs7435827
geneviewrs7435827
scholarrs7435827
googlers7435827
pharmgkbrs7435827
gwascentralrs7435827
openSNPrs7435827
23andMers7435827
23andMe allrs7435827
SNP Nexus

SNPshotrs7435827
SNPdbers7435827
MSV3drs7435827
GWAS Ctlgrs7435827
GMAF0.4187
Max Magnitude
? (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."