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rs8100018

From SNPedia

Orientationplus
Stabilizedplus
Make rs8100018(C;C)
Make rs8100018(C;G)
Make rs8100018(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position40246116
GeneAKT2
is asnp
is mentioned by
dbSNPrs8100018
ebirs8100018
HLIrs8100018
Exacrs8100018
Varsomers8100018
Maprs8100018
PheGenIrs8100018
hapmaprs8100018
1000 genomesrs8100018
hgdprs8100018
ensemblrs8100018
gopubmedrs8100018
geneviewrs8100018
scholarrs8100018
googlers8100018
pharmgkbrs8100018
gwascentralrs8100018
openSNPrs8100018
23andMers8100018
23andMe allrs8100018
SNP Nexus

SNPshotrs8100018
SNPdbers8100018
MSV3drs8100018
GWAS Ctlgrs8100018
GMAF0.3108
Max Magnitude
? (C;C) (C;G) (G;G) 28

[PMID 24421178] PI3K/PTEN/AKT/mTOR pathway genetic variations are associated with the clinical outcome in patients with squamous cell carcinoma of the head and neck receiving cetuximab-docetaxel treatment [PMID 18768676OA-icon.png] First evidence of genetic association between AKT2 and polycystic ovary syndrome.


[PMID 19164214OA-icon.png] Genetic variations in the PI3K/PTEN/AKT/mTOR pathway are associated with clinical outcomes in esophageal cancer patients treated with chemoradiotherapy.