Have questions? Visit https://www.reddit.com/r/SNPedia

rs11938019

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs11938019(C;T)
Make rs11938019(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position68559644
GeneUGT2B17
is asnp
is mentioned by
dbSNPrs11938019
ebirs11938019
HLIrs11938019
Exacrs11938019
Varsomers11938019
Maprs11938019
PheGenIrs11938019
hapmaprs11938019
1000 genomesrs11938019
hgdprs11938019
ensemblrs11938019
gopubmedrs11938019
geneviewrs11938019
scholarrs11938019
googlers11938019
pharmgkbrs11938019
gwascentralrs11938019
openSNPrs11938019
23andMers11938019
23andMe allrs11938019
SNP Nexus

SNPshotrs11938019
SNPdbers11938019
MSV3drs11938019
GWAS Ctlgrs11938019
Max Magnitude0
? (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."