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

rs10138227

From SNPedia

Orientationplus
Make rs10138227(C;C)
Make rs10138227(C;T)
Make rs10138227(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position104793369
GeneAKT1
is asnp
is mentioned by
dbSNPrs10138227
ebirs10138227
HLIrs10138227
Exacrs10138227
Varsomers10138227
Maprs10138227
PheGenIrs10138227
hapmaprs10138227
1000 genomesrs10138227
hgdprs10138227
ensemblrs10138227
gopubmedrs10138227
geneviewrs10138227
scholarrs10138227
googlers10138227
pharmgkbrs10138227
gwascentralrs10138227
openSNPrs10138227
23andMers10138227
23andMe allrs10138227
SNP Nexus

SNPshotrs10138227
SNPdbers10138227
MSV3drs10138227
GWAS Ctlgrs10138227
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 26818920] A Functional Polymorphism (rs2494752) in the AKT1 Promoter Region and Gastric Adenocarcinoma Risk in an Eastern Chinese Population.